A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2663696



Internal ID17774096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:190564..204264hg38UCSC Ensembl
Innerchr19:190564..204264hg19UCSC Ensembl
Innerchr19:141564..155264hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813701
hg1913701
hg1813701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960768
Supporting Variants
SamplesHGDP00542
Known GenesLINC01002
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2663696
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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