A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695546



Internal ID15432198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100051488..100064292hg38UCSC Ensembl
Innerchr14:100517825..100530629hg19UCSC Ensembl
Innerchr14:99587578..99600382hg18UCSC Ensembl
Innerchr14:99587578..99600382hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3812805
hg1912805
hg1812805
hg1712805
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518128
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695546
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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