A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10168



Internal ID15195944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:77235963..77268176hg38UCSC Ensembl
Outerchr18:74947919..74980132hg19UCSC Ensembl
Outerchr18:73076907..73109120hg18UCSC Ensembl
Outerchr18:73076907..73109120hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg387292
hg197292
hg187292
hg177292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2364
Supporting Variants
SamplesNA18956
Known GenesGALR1
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)nssv10168
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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