A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528068



Internal ID15108675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:14117147..14382617hg38UCSC Ensembl
Innerchr12:14270081..14535551hg19UCSC Ensembl
Innerchr12:14161348..14426818hg18UCSC Ensembl
Innerchr12:14161348..14426818hg17UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38265471
hg19265471
hg18265471
hg17265471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704604
Samples
Known GenesATF7IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528068
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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