A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053429



Internal ID19142648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30281095..30376369hg38UCSC Ensembl
Innerchr15:30573298..30668572hg19UCSC Ensembl
Innerchr15:28360590..28455864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3895275
hg1995275
hg1895275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2510n100
Supporting Variantsnssv3546690, nssv3546689
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)nsv1053429
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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