A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1256



Internal ID15544469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68005962..68030865hg38UCSC Ensembl
Outerchr15:68298300..68323203hg19UCSC Ensembl
Outerchr15:66085354..66110257hg18UCSC Ensembl
Outerchr15:66085354..66110257hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg388482
hg198482
hg188482
hg178482
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1579
Supporting Variants
SamplesNA19240
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)nssv1256
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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