A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695635



Internal ID15432287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113901406..113916864hg38UCSC Ensembl
Innerchr10:115661165..115676623hg19UCSC Ensembl
Innerchr10:115651155..115666613hg18UCSC Ensembl
Innerchr10:115651155..115666613hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3815459
hg1915459
hg1815459
hg1715459
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517356
Supporting Variants
Samples
Known GenesNHLRC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695635
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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