A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661487



Internal ID15398139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4395562..4396785hg38UCSC Ensembl
Innerchr10:4437754..4438977hg19UCSC Ensembl
Innerchr10:4427754..4428977hg18UCSC Ensembl
Innerchr10:4427754..4428977hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381224
hg191224
hg181224
hg171224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516066
Supporting Variants
Samples
Known GenesLINC00703
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661487
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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