A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641077



Internal ID6681162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67032340..67042614hg38UCSC Ensembl
Innerchr17:67032340..67042614hg38UCSC Ensembl
Outerchr17:67032219..67042735hg38UCSC Ensembl
chr17:65028456..65038730hg19UCSC Ensembl
Innerchr17:65028456..65038730hg19UCSC Ensembl
Outerchr17:65028335..65038851hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810275
hg1910275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15726577
SamplesNA18566
Known GenesCACNG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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