A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10108



Internal ID15542689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:4875986..4889265hg38UCSC Ensembl
Outerchr17:4779281..4792560hg19UCSC Ensembl
Outerchr17:4725458..4733342hg18UCSC Ensembl
Outerchr17:4725458..4733342hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387786
hg197786
hg187786
hg177786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1953
Supporting Variants
SamplesNA18956
Known GenesMINK1
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)nssv10108
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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