A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705920



Internal ID15095886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72072821..72086126hg38UCSC Ensembl
Innerchr10:73832579..73845884hg19UCSC Ensembl
Innerchr10:73502585..73515890hg18UCSC Ensembl
Innerchr10:73502585..73515890hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813306
hg1913306
hg1813306
hg1713306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522541
Supporting Variants
Samples
Known GenesSPOCK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705920
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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