A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053444



Internal ID19142663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30270555..30376369hg38UCSC Ensembl
Innerchr15:30562758..30668572hg19UCSC Ensembl
Innerchr15:28350050..28455864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38105815
hg19105815
hg18105815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2510n100
Supporting Variantsnssv3546678
Samples
Known GenesCHRFAM7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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