A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960128



Internal ID18595381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59841424..59842255hg38UCSC Ensembl
Innerchr17:57918785..57919616hg19UCSC Ensembl
Innerchr17:55273567..55274398hg18UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38832
hg19832
hg18832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2104012, nssv2104014, nssv2104015, nssv2104009, nssv2104017, nssv2104013, nssv2104016, nssv2104008, nssv2104010, nssv2104011
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960128
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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