A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570941



Internal ID16011664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:173619..175654hg38UCSC Ensembl
Innerchr16:223618..225653hg19UCSC Ensembl
Innerchr16:163618..165653hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382036
hg192036
hg182036
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851286, nssv851285
Samples
Known GenesHBA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570941
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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