A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041765



Internal ID19130984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32274298hg38UCSC Ensembl
Innerchr15:32471475..32566499hg19UCSC Ensembl
Innerchr15:30258767..30353791hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3895025
hg1995025
hg1895025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2539n100
Supporting Variantsnssv3721629
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041765
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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