A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047647



Internal ID18790178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52133682..52176984hg38UCSC Ensembl
Innerchr15:52425879..52469181hg19UCSC Ensembl
Innerchr15:50213171..50256473hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3843303
hg1943303
hg1843303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552403
Samples
Known GenesGNB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047647
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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