A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5003



Internal ID15544018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:93696694..93711210hg38UCSC Ensembl
Outerchr7:93326006..93340522hg19UCSC Ensembl
Outerchr7:93163942..93178458hg18UCSC Ensembl
Outerchr7:92970657..92985173hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3814517
hg1914517
hg1814517
hg1714517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5847
Supporting Variants
SamplesNA19129
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)nssv5003
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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