A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971868



Internal ID16265824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:124886813..124887461hg38UCSC Ensembl
Innerchr3:124605660..124606308hg19UCSC Ensembl
Innerchr3:126088350..126088998hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38649
hg19649
hg18649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591448
Supporting Variants
Samples
Known GenesITGB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv971868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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