A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1856982



Internal ID17845178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73242870..73243833hg38UCSC Ensembl
Innerchr10:75002628..75003591hg19UCSC Ensembl
Innerchr10:74672634..74673597hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948066
Supporting Variants
SamplesHGDP01029
Known GenesDNAJC9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1856982
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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