A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149539



Internal ID15508051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92685875..92724438hg38UCSC Ensembl
Innerchr14:93152220..93190783hg19UCSC Ensembl
Innerchr14:92221973..92260536hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3838564
hg1938564
hg1838564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565524
Supporting Variants
Samples1780862306_A
Known GenesLGMN, RIN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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