A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038958



Internal ID18781489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313356..30529543hg38UCSC Ensembl
Innerchr15:30605559..30821746hg19UCSC Ensembl
Innerchr15:28392851..28609038hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38216188
hg19216188
hg18216188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3546759
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038958
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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