A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981442



Internal ID18616639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25206627..25214475hg38UCSC Ensembl
Innerchr7:25246246..25254094hg19UCSC Ensembl
Innerchr7:25212771..25220619hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg387849
hg197849
hg187849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2439184, nssv2439179, nssv2439180, nssv2439178, nssv2439182, nssv2439176, nssv2439183, nssv2439177, nssv2439181, nssv2439185
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)nsv981442
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