A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054764



Internal ID18797295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40776427..40904212hg38UCSC Ensembl
Innerchr15:41068625..41196410hg19UCSC Ensembl
Innerchr15:38855917..38983702hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38127786
hg19127786
hg18127786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552251
Samples
Known GenesDNAJC17, PPP1R14D, RHOV, SPINT1, VPS18, ZFYVE19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054764
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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