A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10357



Internal ID15542441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:175077276..175125270hg38UCSC Ensembl
Outerchr1:175046412..175094406hg19UCSC Ensembl
Outerchr1:173313035..173361029hg18UCSC Ensembl
Outerchr1:171778069..171826063hg17UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3847995
hg1947995
hg1847995
hg1747995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3609
Supporting Variants
SamplesNA18956
Known GenesTNN
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)nssv10357
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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