A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665592



Internal ID9931697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81519506..81520244hg38UCSC Ensembl
Outerchr17:81519469..81520294hg38UCSC Ensembl
Innerchr17:79486532..79487270hg19UCSC Ensembl
Outerchr17:79486495..79487320hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6544778
SamplesNA20502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665592
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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