A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9725



Internal ID15539968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:105742868..105766831hg38UCSC Ensembl
Outerchr7:105383314..105407277hg19UCSC Ensembl
Outerchr7:105170550..105194513hg18UCSC Ensembl
Outerchr7:104977265..105001228hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3812736
hg1912736
hg1812736
hg1712736
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890
Supporting Variants
SamplesNA18507
Known GenesATXN7L1
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)nssv9725
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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