A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv925606



Internal ID16219562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:172424511..172443028hg38UCSC Ensembl
Innerchr2:173289239..173307756hg19UCSC Ensembl
Innerchr2:172997485..173016002hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3818518
hg1918518
hg1818518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583664
Supporting Variants
Samples
Known GenesITGA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv925606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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