A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904254



Internal ID6266181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57707259..60018487hg19UCSC Ensembl
Outerchr15:57702953..60021637hg19UCSC Ensembl
Innerchr15:55494551..57805779hg18UCSC Ensembl
Outerchr15:55490245..57808929hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1555644
SamplesMS21477
Known GenesADAM10, ALDH1A2, AQP9, BNIP2, CCNB2, CGNL1, FAM63B, FAM81A, GCNT3, GCOM1, GRINL1A, GTF2A2, HSP90AB4P, LDHAL6B, LIPC, MIR2116, MYO1E, RNF111, SLTM
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904254
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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