A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726030



Internal ID19024311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51887038..52151161hg38UCSC Ensembl
Innerchr2:52114176..52378299hg19UCSC Ensembl
Innerchr2:51967680..52231803hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38264124
hg19264124
hg18264124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014342
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)nssv3726030
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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