A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2731601

Internal ID9965919
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:13230788..13231666hg38UCSC Ensembl
Outerchr6:13231020..13231898hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6947711, essv6727040, essv6700968, essv6890129, essv6974648, essv6778093, essv6822374, essv6704907, essv6893423, essv6963599, essv6918659, essv6671003, essv6814238, essv6719323, essv6778094, essv6869604, essv6683928, essv6865490, essv6830100, essv6818111, essv6943270, essv6837341, essv6826296, essv6782097, essv6676460, essv6786297, essv6759697, essv6694072, essv6811224, essv6878539, essv6907449, essv6794568, essv6860722, essv6711751, essv6690339, essv6697856, essv6886946, essv6805335, essv6956871, essv6848999, essv6808314, essv6677555, essv6790419, essv6855114, essv6757328
SamplesSSM027, SSM086, SSM036, SSM042, SSM040, SSM078, SSM088, SSM089, SSM090, SSM031, SSM071, SSM032, SSM039, SSM024, SSM067, SSM083, SSM097, SSM077, SSM005, SSM093, SSM017, SSM029, SSM069, SSM037, SSM034, SSM087, SSM038, SSM046, SSM096, SSM023, SSM079, SSM068, SSM044, SSM074, SSM075, SSM026, SSM014, SSM008, SSM098, SSM076, SSM059, SSM081, SSM070, SSM080
Known GenesPHACTR1
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Pubmed ID23290073
Accession Number(s)esv2731601
Sample Size96
Observed Gain0
Observed Loss44
Observed Complex0

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