A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527307



Internal ID15107914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58811129..59726288hg38UCSC Ensembl
Innerchr15:59103328..60018487hg19UCSC Ensembl
Innerchr15:56890620..57805779hg18UCSC Ensembl
Innerchr15:56890620..57805779hg17UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38915160
hg19915160
hg18915160
hg17915160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703727
Samples
Known GenesBNIP2, CCNB2, FAM63B, FAM81A, GCNT3, GTF2A2, LDHAL6B, MIR2116, MYO1E, RNF111, SLTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527307
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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