A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8409



Internal ID15535455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101090767..101101191hg38UCSC Ensembl
Outerchr7:100734048..100744472hg19UCSC Ensembl
Outerchr7:100520768..100531192hg18UCSC Ensembl
Outerchr7:100327483..100337907hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810425
hg1910425
hg1810425
hg1710425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874
Supporting Variants
SamplesNA12156
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)nssv8409
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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