A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967766



Internal ID18602994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76401169..76401669hg38UCSC Ensembl
Innerchr4:77322322..77322822hg19UCSC Ensembl
Innerchr4:77541346..77541846hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2324304, nssv2324303, nssv2324309, nssv2324307, nssv2324308, nssv2324306, nssv2324302, nssv2324310, nssv2324305, nssv2324301
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC158
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967766
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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