A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15657897



Internal ID6780426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31065095..31070767hg38UCSC Ensembl
Innerchr17:31065125..31070737hg38UCSC Ensembl
Outerchr17:31065065..31070797hg38UCSC Ensembl
chr17:29392113..29397785hg19UCSC Ensembl
Innerchr17:29392143..29397755hg19UCSC Ensembl
Outerchr17:29392083..29397815hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640359
Supporting Variants
SamplesNA20881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15657897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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