A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704552



Internal ID15441204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52360896..52363004hg38UCSC Ensembl
Innerchr14:52827614..52829722hg19UCSC Ensembl
Innerchr14:51897364..51899472hg18UCSC Ensembl
Innerchr14:51897364..51899472hg17UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg382109
hg192109
hg182109
hg172109
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528023
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704552
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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