A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765716



Internal ID17755947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122587690..122592000hg38UCSC Ensembl
Innerchr10:124347206..124351516hg19UCSC Ensembl
Innerchr10:124337196..124341506hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384311
hg194311
hg184311
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv971857
Supporting Variants
SamplesHGDP00521
Known GenesDMBT1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765716
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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