A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149664



Internal ID15532640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89091139..89174375hg38UCSC Ensembl
Innerchr16:89157547..89240783hg19UCSC Ensembl
Innerchr16:87685048..87768284hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3883237
hg1983237
hg1883237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573723
Supporting Variants
SamplesHGDP01346
Known GenesACSF3, CDH15, LINC00304, LOC400558
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149664
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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