A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961210



Internal ID18249770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34293184..34296769hg38UCSC Ensembl
Innerchr19:34784089..34787674hg19UCSC Ensembl
Innerchr19:39475929..39479514hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383586
hg193586
hg183586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145230, nssv2145232, nssv2145231, nssv2145227, nssv2145225, nssv2145223, nssv2145226, nssv2145228, nssv2145229, nssv2145224
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesKIAA0355
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961210
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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