A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961222



Internal ID18249782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42619215..42620003hg38UCSC Ensembl
Innerchr19:43123367..43124155hg19UCSC Ensembl
Innerchr19:47815207..47815995hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38789
hg19789
hg18789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2150783, nssv2150787, nssv2150781, nssv2150786, nssv2150785, nssv2150788, nssv2150782, nssv2150779, nssv2150784, nssv2150780
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLIPE-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961222
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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