A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1570



Internal ID15199447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:65086777..65105393hg38UCSC Ensembl
Outerchr15:65379115..65397731hg19UCSC Ensembl
Outerchr15:63166168..63184784hg18UCSC Ensembl
Outerchr15:63166168..63184784hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385679
hg195679
hg185679
hg175679
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7187
SamplesNA12156
Known GenesUBAP1L
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)nsv1570
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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