A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681860



Internal ID15418512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146556961..146557568hg38UCSC Ensembl
Innerchr7:146254053..146254660hg19UCSC Ensembl
Innerchr7:145884986..145885593hg18UCSC Ensembl
Innerchr7:145691701..145692308hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38608
hg19608
hg18608
hg17608
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515777
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681860
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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