A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149537



Internal ID15530644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91297293..91330777hg38UCSC Ensembl
Innerchr14:91763637..91797121hg19UCSC Ensembl
Innerchr14:90833390..90866874hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3833485
hg1933485
hg1833485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565518
Supporting Variants
SamplesHGDP00970
Known GenesCCDC88C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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