A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2655452



Internal ID17744425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26978507..26982040hg38UCSC Ensembl
Innerchr17:25305533..25309066hg19UCSC Ensembl
Innerchr17:22329660..22333193hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg383534
hg193534
hg183534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv960172
Supporting Variants
SamplesHGDP00521
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)nssv2655452
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