A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4964



Internal ID15544080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:6065831..6107517hg38UCSC Ensembl
Outerchr7:6105462..6147148hg19UCSC Ensembl
Outerchr7:6071988..6113674hg18UCSC Ensembl
Outerchr7:5878703..5920389hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3841687
hg1941687
hg1841687
hg1741687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5628
Supporting Variants
SamplesNA19129
Known GenesUSP42
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4964
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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