A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2157291



Internal ID17835857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53085976..53086904hg38UCSC Ensembl
Innerchr19:53589229..53590157hg19UCSC Ensembl
Innerchr19:58281041..58281969hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38929
hg19929
hg18929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv978844
Supporting Variants
SamplesHGDP00998
Known GenesZNF160
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2157291
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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