A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058708



Internal ID18801239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88040927..88082524hg38UCSC Ensembl
Innerchr16:88074533..88116130hg19UCSC Ensembl
Innerchr16:86632034..86673631hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3841598
hg1941598
hg1841598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559983
Samples
Known GenesBANP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058708
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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