A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1835560



Internal ID17794437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21027697..21030987hg38UCSC Ensembl
Innerchr10:21316626..21319916hg19UCSC Ensembl
Innerchr10:21356632..21359922hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383291
hg193291
hg183291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947763
Supporting Variants
SamplesHGDP00778
Known GenesNEBL
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)nssv1835560
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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