A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948188



Internal ID18248348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:112547790..112549521hg38UCSC Ensembl
Innerchr10:114307549..114309280hg19UCSC Ensembl
Innerchr10:114297539..114299270hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381732
hg191732
hg181732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1867688, nssv1867695, nssv1867694, nssv1867693, nssv1867691, nssv1867696, nssv1867689, nssv1867690, nssv1867692, nssv1867687
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesVTI1A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948188
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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