A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148976



Internal ID15528924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99549708..99559838hg38UCSC Ensembl
Innerchr14:100016045..100026175hg19UCSC Ensembl
Innerchr14:99085798..99095928hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810131
hg1910131
hg1810131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565734
Supporting Variants
SamplesHGDP00708
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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