A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653



Internal ID15545213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91575772..91622111hg38UCSC Ensembl
Outerchr7:91205087..91251426hg19UCSC Ensembl
Outerchr7:91043023..91089362hg18UCSC Ensembl
Outerchr7:90849738..90896077hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3846340
hg1946340
hg1846340
hg1746340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835
Supporting Variants
SamplesNA19240
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)nssv653
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