A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947859



Internal ID18594706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38344519..38385618hg38UCSC Ensembl
Innerchr10:38633447..38674546hg19UCSC Ensembl
Innerchr10:38673453..38714552hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3841100
hg1941100
hg1841100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1842393, nssv1842394, nssv1842392, nssv1842390, nssv1842396, nssv1842395, nssv1842388, nssv1842391, nssv1842397, nssv1842389
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHSD17B7P2, SEPT7P9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947859
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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