A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967783



Internal ID18256325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109594256..109596664hg38UCSC Ensembl
Innerchr4:110515412..110517820hg19UCSC Ensembl
Innerchr4:110734861..110737269hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg382409
hg192409
hg182409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2331105, nssv2331102, nssv2331103, nssv2331101, nssv2331100, nssv2331108, nssv2331106, nssv2331107, nssv2331104, nssv2331109
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC109B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967783
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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