A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663177



Internal ID15399829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23100321..23104578hg38UCSC Ensembl
Innerchr7:23139940..23144197hg19UCSC Ensembl
Innerchr7:23106465..23110722hg18UCSC Ensembl
Innerchr7:22913180..22917437hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384258
hg194258
hg184258
hg174258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516984
Supporting Variants
Samples
Known GenesKLHL7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663177
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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