A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672583



Internal ID15062549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86921241..86973435hg38UCSC Ensembl
Innerchr10:88680998..88733192hg19UCSC Ensembl
Innerchr10:88670978..88723172hg18UCSC Ensembl
Innerchr10:88670978..88723172hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3852195
hg1952195
hg1852195
hg1752195
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517487
Supporting Variants
Samples
Known GenesADIRF, AGAP11, BMPR1A, MMRN2, SNCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672583
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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