A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702914



Internal ID15439566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61146788..61148022hg38UCSC Ensembl
Innerchr14:61613506..61614740hg19UCSC Ensembl
Innerchr14:60683259..60684493hg18UCSC Ensembl
Innerchr14:60683259..60684493hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381235
hg191235
hg181235
hg171235
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526595
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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