A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037664



Internal ID18780195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:93505..171058hg38UCSC Ensembl
Innerchr16:143503..221057hg19UCSC Ensembl
Innerchr16:83503..161057hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3877554
hg1977555
hg1877555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556942
Samples
Known GenesHBM, HBZ, NPRL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037664
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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