A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971857



Internal ID18607074
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761571, nssv2765716, nssv2762484, nssv2759399, nssv2761445, nssv2761150, nssv2758936, nssv2762104
SamplesHGDP01284, HGDP00998, HGDP00521, HGDP00778, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDMBT1
MethodSequencing
AnalysisGorilla CNVs
Human CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971857
Frequency
Sample Size10
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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