A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967784



Internal ID18603012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109673519..109680825hg38UCSC Ensembl
Innerchr4:110594675..110601981hg19UCSC Ensembl
Innerchr4:110814124..110821430hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg387307
hg197307
hg187307
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2331133, nssv2331137, nssv2331142, nssv2331136, nssv2331135, nssv2331138, nssv2331141, nssv2331134, nssv2331140, nssv2331139
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)nsv967784
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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