A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825759



Internal ID16119715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35534330..35535507hg38UCSC Ensembl
Innerchr14:36003536..36004713hg19UCSC Ensembl
Innerchr14:35073287..35074464hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381178
hg191178
hg181178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564337
Supporting Variants
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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