A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702726



Internal ID15092692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105312968..105439736hg38UCSC Ensembl
Innerchr14:105779305..105906073hg19UCSC Ensembl
Innerchr14:104850350..104977118hg18UCSC Ensembl
Innerchr14:104850350..104977118hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38126769
hg19126769
hg18126769
hg17126769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesBRF1, MTA1, PACS2, TEX22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702726
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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