A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761943



Internal ID17482754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122833633..122836634hg38UCSC Ensembl
Innerchr10:124593149..124596150hg19UCSC Ensembl
Innerchr10:124583139..124586140hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383002
hg193002
hg183002
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975804
Supporting Variants
SamplesHGDP00998
Known GenesCUZD1, FAM24B-CUZD1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761943
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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