A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960522



Internal ID18595773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64970798..64997984hg38UCSC Ensembl
Innerchr17:62966916..62994102hg19UCSC Ensembl
Innerchr17:60397378..60424564hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3827187
hg1927187
hg1827187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2108504, nssv2108498, nssv2108496, nssv2108495, nssv2108503, nssv2108499, nssv2108500, nssv2108502, nssv2108501, nssv2108497
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAMZ2P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960522
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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