A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1837700



Internal ID17480869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28521083..28523400hg38UCSC Ensembl
Innerchr10:28810012..28812329hg19UCSC Ensembl
Innerchr10:28850018..28852335hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg382318
hg192318
hg182318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947797
Supporting Variants
SamplesHGDP00998
Known GenesWAC-AS1
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)nssv1837700
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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