A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6720



Internal ID15190458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41938368..41975161hg38UCSC Ensembl
Outerchr17:40094621..40127179hg19UCSC Ensembl
Outerchr17:37348147..37380705hg18UCSC Ensembl
Outerchr17:37348147..37380705hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg386881
hg196881
hg186881
hg176881
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2056
Supporting Variants
SamplesNA12156
Known GenesCNP, TTC25
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)nssv6720
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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