A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523532



Internal ID15450825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:212862216..212863657hg38UCSC Ensembl
Innerchr2:213726940..213728381hg19UCSC Ensembl
Innerchr2:213435185..213436626hg18UCSC Ensembl
Innerchr2:213552446..213553887hg17UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg381442
hg191442
hg181442
hg171442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699307
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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