A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013079



Internal ID18755610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46722198..46771278hg38UCSC Ensembl
Innerchr2:46949337..46998417hg19UCSC Ensembl
Innerchr2:46802841..46851921hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3849081
hg1949081
hg1849081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581632
Samples
Known GenesSOCS5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013079
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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