A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732586



Internal ID16026542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190706406..190778771hg38UCSC Ensembl
Innerchr1:190675536..190747901hg19UCSC Ensembl
Innerchr1:188942159..189014524hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3872366
hg1972366
hg1872366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548570
Supporting Variants
Samples
Known GenesLOC440704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv732586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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