A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948135



Internal ID18594981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91663270..91670463hg38UCSC Ensembl
Innerchr10:93423027..93430220hg19UCSC Ensembl
Innerchr10:93413007..93420200hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg387194
hg197194
hg187194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862993, nssv1862996, nssv1862990, nssv1862995, nssv1862992, nssv1862989, nssv1862991, nssv1862994, nssv1862987, nssv1862988
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948135
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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