A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683632



Internal ID15420284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23106333..23106570hg38UCSC Ensembl
Innerchr7:23145952..23146189hg19UCSC Ensembl
Innerchr7:23112477..23112714hg18UCSC Ensembl
Innerchr7:22919192..22919429hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38238
hg19238
hg18238
hg17238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516984
Supporting Variants
Samples
Known GenesKLHL7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer