A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570494



Internal ID18868775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12772..176399hg38UCSC Ensembl
Innerchr2:12772..176399hg19UCSC Ensembl
Innerchr2:2772..166399hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38163628
hg19163628
hg18163628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998709
Supporting Variants
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3570494
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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