A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729888



Internal ID19028169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88861741..89222453hg38UCSC Ensembl
Innerchr2:89161253..89521934hg19UCSC Ensembl
Innerchr2:88942368..89303049hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38360713
hg19360682
hg18360682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013480
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)nssv3729888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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