A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726032



Internal ID19024313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52221523..52361637hg38UCSC Ensembl
Innerchr2:52448661..52588775hg19UCSC Ensembl
Innerchr2:52302165..52442279hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38140115
hg19140115
hg18140115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999967
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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