A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2655667



Internal ID17494625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27466314..27468682hg38UCSC Ensembl
Innerchr17:25793340..25795708hg19UCSC Ensembl
Innerchr17:22817467..22819835hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg382369
hg192369
hg182369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv978494
Supporting Variants
SamplesHGDP00998
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)nssv2655667
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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