A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043884



Internal ID19133103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381218..20422227hg38UCSC Ensembl
Innerchr15:20586471..20627480hg19UCSC Ensembl
Innerchr15:18846485..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3841010
hg1941010
hg1841010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3714737, nssv3714738
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043884
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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