A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697585



Internal ID15434237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99609301..99613129hg38UCSC Ensembl
Innerchr3:99328145..99331973hg19UCSC Ensembl
Innerchr3:100810835..100814663hg18UCSC Ensembl
Innerchr3:100810835..100814663hg17UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg383829
hg193829
hg183829
hg173829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520742
Supporting Variants
Samples
Known GenesMIR548G
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697585
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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