A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703619



Internal ID15093585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73048287..73134617hg38UCSC Ensembl
Innerchr10:74808045..74894375hg19UCSC Ensembl
Innerchr10:74478051..74564381hg18UCSC Ensembl
Innerchr10:74478051..74564381hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3886331
hg1986331
hg1886331
hg1786331
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527219
Supporting Variants
Samples
Known GenesECD, NUDT13, P4HA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703619
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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