A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2440035



Internal ID17804246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25065681..25068031hg38UCSC Ensembl
Innerchr7:25105300..25107650hg19UCSC Ensembl
Innerchr7:25071825..25074175hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382351
hg192351
hg182351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv981441
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2440035
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