A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2932



Internal ID15194936
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
hg386276
hg196276
hg186276
hg176276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1520
Supporting Variants
SamplesNA18555
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)nssv2932
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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