A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7199



Internal ID15189979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76206324..76240497hg38UCSC Ensembl
Outerchr15:76498665..76532838hg19UCSC Ensembl
Outerchr15:74285720..74319893hg18UCSC Ensembl
Outerchr15:74285720..74319893hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg385264
hg195264
hg185264
hg175264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1618
Supporting Variants
SamplesNA12156
Known GenesETFA
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)nssv7199
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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