A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053505



Internal ID19142724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36188791..36260793hg38UCSC Ensembl
Innerchr15:36480992..36552994hg19UCSC Ensembl
Innerchr15:34268284..34340286hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3872003
hg1972003
hg1872003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552232
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)nsv1053505
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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