A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2638214



Internal ID17526994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32479361..32592626hg38UCSC Ensembl
Innerchr16:32490682..32603947hg19UCSC Ensembl
Innerchr16:32398183..32511448hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38113266
hg19113266
hg18113266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv978232
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2638214
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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