A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705179



Internal ID15441831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100051488..100056190hg38UCSC Ensembl
Innerchr14:100517825..100522527hg19UCSC Ensembl
Innerchr14:99587578..99592280hg18UCSC Ensembl
Innerchr14:99587578..99592280hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384703
hg194703
hg184703
hg174703
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705179
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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