A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2627072



Internal ID17776459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10001..19367hg38UCSC Ensembl
Innerchr16:60001..69367hg19UCSC Ensembl
Innerchr16:1..9367hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389367
hg199367
hg189367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv974743
Supporting Variants
SamplesHGDP00542
Known GenesDDX11L10, LOC100288778, MIR6859-1, MIR6859-2
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2627072
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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