A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705838



Internal ID15442490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36937811..36950668hg38UCSC Ensembl
Innerchr1:37403412..37416269hg19UCSC Ensembl
Innerchr1:37175999..37188856hg18UCSC Ensembl
Innerchr1:37072505..37085362hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812858
hg1912858
hg1812858
hg1712858
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522473
Supporting Variants
Samples
Known GenesGRIK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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