A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960533



Internal ID18249098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76679837..76681031hg38UCSC Ensembl
Innerchr17:74675919..74677113hg19UCSC Ensembl
Innerchr17:72187514..72188708hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381195
hg191195
hg181195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2111735, nssv2111736, nssv2111733, nssv2111732, nssv2111734, nssv2110939, nssv2110936, nssv2111737, nssv2110938, nssv2110937
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesMXRA7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960533
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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