A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047375



Internal ID18789906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23396355..23452098hg38UCSC Ensembl
Innerchr15:23641502..23697245hg19UCSC Ensembl
Innerchr15:21192943..21248338hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3855744
hg1955744
hg1855396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538885
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)nsv1047375
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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