A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700424



Internal ID15437076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23027525..23180616hg38UCSC Ensembl
Innerchr7:23067144..23220235hg19UCSC Ensembl
Innerchr7:23033669..23186760hg18UCSC Ensembl
Innerchr7:22840384..22993475hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38153092
hg19153092
hg18153092
hg17153092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524486
Supporting Variants
Samples
Known GenesKLHL7, KLHL7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700424
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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