A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1635



Internal ID15198747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161459185..161502526hg38UCSC Ensembl
Outerchr1:161428975..161472316hg19UCSC Ensembl
Outerchr1:159695599..159738940hg18UCSC Ensembl
Outerchr1:158242030..158285371hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3843342
hg1943342
hg1843342
hg1743342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243
Supporting Variants
SamplesNA19240
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)nssv1635
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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