A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050722



Internal ID19139941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70674404..70714570hg38UCSC Ensembl
Innerchr15:70966743..71006909hg19UCSC Ensembl
Innerchr15:68753797..68793963hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3840167
hg1940167
hg1840167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2618n100
Supporting Variantsnssv3553673
Samples
Known GenesUACA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050722
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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