A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1858362



Internal ID17498568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73005748..73007736hg38UCSC Ensembl
Innerchr10:74765506..74767494hg19UCSC Ensembl
Innerchr10:74435512..74437500hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381989
hg191989
hg181989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948064
Supporting Variants
SamplesHGDP01029
Known GenesP4HA1
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)nssv1858362
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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