A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2615792



Internal ID17812831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73681394..73682009hg38UCSC Ensembl
Innerchr10:75441152..75441767hg19UCSC Ensembl
Innerchr10:75111158..75111773hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38616
hg19616
hg18616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975705
Supporting Variants
SamplesHGDP00927
Known GenesAGAP5
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)nssv2615792
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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