A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904640



Internal ID15851910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32628589..32684857hg38UCSC Ensembl
Innerchr2:32853656..32909924hg19UCSC Ensembl
Innerchr2:32707160..32763428hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3856269
hg1956269
hg1856269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581283
Supporting Variants
Samples
Known GenesMIR4765, TTC27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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