A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739189



Internal ID9973530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133895816..133896178hg38UCSC Ensembl
Outerchr9:136760938..136761300hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6795615, essv6850536, essv6952797, essv6740726, essv6757956, essv6895610, essv6965114, essv6976367, essv6887694, essv6727950
SamplesSSM059, SSM071, SSM027, SSM046, SSM029, SSM096, SSM086, SSM025, SSM052, SSM012
Known GenesVAV2
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2739189
Frequency
Sample Size96
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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