A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998661



Internal ID19158197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13585769..13633387hg38UCSC Ensembl
Innerchr2:13725894..13773512hg19UCSC Ensembl
Innerchr2:13643345..13690963hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3847619
hg1947619
hg1847619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726793
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)nsv998661
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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