A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521667



Internal ID15102274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34696031..34966937hg38UCSC Ensembl
Innerchr10:34984959..35255865hg19UCSC Ensembl
Innerchr10:35024965..35295871hg18UCSC Ensembl
Innerchr10:35024965..35295871hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38270907
hg19270907
hg18270907
hg17270907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698286
Samples
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521667
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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