A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948095



Internal ID18594941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79801605..79919785hg38UCSC Ensembl
Innerchr10:81561361..81679541hg19UCSC Ensembl
Innerchr10:81543948..81669521hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38118181
hg19118181
hg18125574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1859189, nssv1859195, nssv1859197, nssv1859192, nssv1859191, nssv1859190, nssv1859196, nssv1859188, nssv1859193, nssv1859194
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC100288974, LOC642361
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948095
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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