A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019



Internal ID15550886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156577435..156602441hg38UCSC Ensembl
Outerchr7:156370129..156395135hg19UCSC Ensembl
Outerchr7:156062890..156087896hg18UCSC Ensembl
Outerchr7:155869605..155894611hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3825007
hg1925007
hg1825007
hg1725007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3601
SamplesNA12878
Known GenesLINC01006
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)nsv6019
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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