A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981508



Internal ID18616705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66476370..66493749hg38UCSC Ensembl
Innerchr7:65941357..65958736hg19UCSC Ensembl
Innerchr7:65578792..65596171hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3817380
hg1917380
hg1817380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2459951, nssv2459947, nssv2459945, nssv2459944, nssv2459948, nssv2459950, nssv2459952, nssv2459946, nssv2459949, nssv2459953
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981508
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer