A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981440



Internal ID18616637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23585237..23586339hg38UCSC Ensembl
Innerchr7:23624856..23625958hg19UCSC Ensembl
Innerchr7:23591381..23592483hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381103
hg191103
hg181103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2438957, nssv2438952, nssv2438951, nssv2438958, nssv2438950, nssv2438953, nssv2438956, nssv2438954, nssv2438955, nssv2438959
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCLK2P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981440
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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