A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640447



Internal ID7027222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35353525..35442202hg38UCSC Ensembl
Innerchr17:35353675..35442052hg38UCSC Ensembl
Outerchr17:35353375..35442352hg38UCSC Ensembl
chr17:33680544..33769221hg19UCSC Ensembl
Innerchr17:33680694..33769071hg19UCSC Ensembl
Outerchr17:33680394..33769371hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3888678
hg1988678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv570e214
Supporting Variantsessv15664517, essv15664516, essv15664519, essv15664520, essv15664518, essv15664515
SamplesHG00351, HG00338, NA06989, HG00265, HG01269, HG00372
Known GenesSLFN11, SLFN12, SLFN13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640447
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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