A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690091



Internal ID15426743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113901406..113920236hg38UCSC Ensembl
Innerchr10:115661165..115679995hg19UCSC Ensembl
Innerchr10:115651155..115669985hg18UCSC Ensembl
Innerchr10:115651155..115669985hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3818831
hg1918831
hg1818831
hg1718831
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)nssv690091
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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