A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690419



Internal ID15427071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23100321..23106333hg38UCSC Ensembl
Innerchr7:23139940..23145952hg19UCSC Ensembl
Innerchr7:23106465..23112477hg18UCSC Ensembl
Innerchr7:22913180..22919192hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386013
hg196013
hg186013
hg176013
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516984
Supporting Variants
Samples
Known GenesKLHL7, KLHL7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690419
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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