A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525679



Internal ID15452972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:91525159..91531223hg38UCSC Ensembl
Innerchr14:91991503..91997567hg19UCSC Ensembl
Innerchr14:91061256..91067320hg18UCSC Ensembl
Innerchr14:91061256..91067320hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386065
hg196065
hg186065
hg176065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701837
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525679
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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