A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2708128



Internal ID17878843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:39797842..39799704hg38UCSC Ensembl
Innerchr7:39837441..39839303hg19UCSC Ensembl
Innerchr7:39803966..39805828hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381863
hg191863
hg181863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970997
Supporting Variants
SamplesHGDP01307
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2708128
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