A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7953



Internal ID15535911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:202639292..202667502hg38UCSC Ensembl
Outerchr1:202608420..202636630hg19UCSC Ensembl
Outerchr1:200875043..200903253hg18UCSC Ensembl
Outerchr1:199340077..199368287hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386495
hg196495
hg186495
hg176495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4099
Supporting Variants
SamplesNA12156
Known GenesSYT2
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)nssv7953
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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