A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2619826



Internal ID17778887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18851206..18851934hg38UCSC Ensembl
Innerchr13:19425346..19426074hg19UCSC Ensembl
Innerchr13:18323346..18324074hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38729
hg19729
hg18729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976160
Supporting Variants
SamplesHGDP00665
Known GenesANKRD20A9P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2619826
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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