A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2609441



Internal ID17808388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45677903..45682225hg38UCSC Ensembl
Innerchr10:46173351..46177673hg19UCSC Ensembl
Innerchr10:45493357..45497679hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg384323
hg194323
hg184323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975681
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2609441
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer