A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1520



Internal ID15199397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45354025..45387779hg38UCSC Ensembl
Outerchr15:45646223..45679977hg19UCSC Ensembl
Outerchr15:43433515..43467269hg18UCSC Ensembl
Outerchr15:43433515..43467269hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg386010
hg196010
hg186010
hg176010
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7163, nssv2932
SamplesNA12156, NA18555
Known GenesGATM, GATM-AS1
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)nsv1520
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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