A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10467



Internal ID15195645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:209902256..209920906hg38UCSC Ensembl
Outerchr1:210075601..210094251hg19UCSC Ensembl
Outerchr1:208142224..208160874hg18UCSC Ensembl
Outerchr1:206463996..206482646hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3818651
hg1918651
hg1818651
hg1718651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4354
Supporting Variants
SamplesNA18956
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)nssv10467
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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