A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149536



Internal ID15533116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91276314..91332346hg38UCSC Ensembl
Innerchr14:91742658..91798690hg19UCSC Ensembl
Innerchr14:90812411..90868443hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3856033
hg1956033
hg1856033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565517
Supporting Variants
SamplesNINDS_111
Known GenesCCDC88C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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