A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058997



Internal ID19148216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35468311hg38UCSC Ensembl
Innerchr16:34470704..34702682hg19UCSC Ensembl
Innerchr16:34328205..34560183hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38231979
hg19231979
hg18231979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3722469, nssv3558370
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058997
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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