A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv732587



Internal ID16026543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190706406..190804699hg38UCSC Ensembl
Innerchr1:190675536..190773829hg19UCSC Ensembl
Innerchr1:188942159..189040452hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3898294
hg1998294
hg1898294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548572
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)nssv732587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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