A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702911



Internal ID15439563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158054709..158056749hg38UCSC Ensembl
Innerchr1:158024499..158026539hg19UCSC Ensembl
Innerchr1:156291123..156293163hg18UCSC Ensembl
Innerchr1:154837572..154839612hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382041
hg192041
hg182041
hg172041
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526592
Supporting Variants
Samples
Known GenesKIRREL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702911
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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