A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700382



Internal ID15090348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161711078..161711990hg38UCSC Ensembl
Innerchr1:161680868..161681780hg19UCSC Ensembl
Innerchr1:159947492..159948404hg18UCSC Ensembl
Innerchr1:158412526..158413438hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38913
hg19913
hg18913
hg17913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524449
Supporting Variants
Samples
Known GenesFCRLA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700382
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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