A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149509



Internal ID15853835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85960618..86033755hg38UCSC Ensembl
Innerchr14:86426962..86500099hg19UCSC Ensembl
Innerchr14:85496715..85569852hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3873138
hg1973138
hg1873138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565453
Supporting Variants
Samples1780854459_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149509
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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