A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947817



Internal ID18594664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31364251..31365952hg38UCSC Ensembl
Innerchr10:31653180..31654881hg19UCSC Ensembl
Innerchr10:31693186..31694887hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381702
hg191702
hg181702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2606710, nssv1836814, nssv2606715, nssv1836811, nssv1836812, nssv2606711, nssv2606714, nssv1836815, nssv2605326, nssv2606708, nssv1836813, nssv1836817, nssv2606712, nssv2606709, nssv1836810, nssv1836816, nssv1836808, nssv2606713, nssv2605325, nssv1836809
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZEB1
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947817
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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