A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2445862



Internal ID17806948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39866778..39873693hg38UCSC Ensembl
Innerchr7:39906377..39913292hg19UCSC Ensembl
Innerchr7:39872902..39879817hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386916
hg196916
hg186916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv970469
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2445862
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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