A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148628



Internal ID15875694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:82948760..82977351hg38UCSC Ensembl
Innerchr14:83415104..83443695hg19UCSC Ensembl
Innerchr14:82484857..82513448hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3828592
hg1928592
hg1828592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565334
Supporting Variants
SamplesHGDP00723
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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