A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2671



Internal ID15540437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91573135..91595637hg38UCSC Ensembl
Outerchr7:91202450..91224952hg19UCSC Ensembl
Outerchr7:91040386..91062888hg18UCSC Ensembl
Outerchr7:90847101..90869603hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3822503
hg1922503
hg1822503
hg1722503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835
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)nssv2671
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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