A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2673



Internal ID15540434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93771016..93817391hg38UCSC Ensembl
Outerchr7:93400328..93446703hg19UCSC Ensembl
Outerchr7:93238264..93284639hg18UCSC Ensembl
Outerchr7:93044979..93091354hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3846376
hg1946376
hg1846376
hg1746376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848
Supporting Variants
SamplesNA18555
Known Genes
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)nssv2673
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