A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695575



Internal ID15085541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70839740..70843134hg38UCSC Ensembl
Innerchr10:72599497..72602891hg19UCSC Ensembl
Innerchr10:72269503..72272897hg18UCSC Ensembl
Innerchr10:72269503..72272897hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383395
hg193395
hg183395
hg173395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517453
Supporting Variants
Samples
Known GenesSGPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695575
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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