A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947898



Internal ID18248059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43629064..43631762hg38UCSC Ensembl
Innerchr10:44124512..44127210hg19UCSC Ensembl
Innerchr10:43444518..43447216hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1843415, nssv1843418, nssv1843413, nssv1843416, nssv1843409, nssv1843412, nssv1843417, nssv1843410, nssv1843414, nssv1843411
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF32-AS3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947898
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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