A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524778



Internal ID15105385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23519577..23521896hg38UCSC Ensembl
Innerchr14:23988786..23991105hg19UCSC Ensembl
Innerchr14:23058626..23060945hg18UCSC Ensembl
Innerchr14:23058626..23060945hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382320
hg192320
hg182320
hg172320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700769
Samples
Known GenesTHTPA, ZFHX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524778
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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