A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678741



Internal ID15068707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65219183..65737334hg38UCSC Ensembl
Innerchr7:64679561..65202326hg19UCSC Ensembl
Innerchr7:64316996..64839761hg18UCSC Ensembl
Innerchr7:64123711..64646476hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38518152
hg19522766
hg18522766
hg17522766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517778
Supporting Variants
Samples
Known GenesINTS4L2, LOC441242, ZNF92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678741
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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