A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7275



Internal ID15205582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2536472..2680329hg38UCSC Ensembl
Outerchr16:2586473..2730330hg19UCSC Ensembl
Outerchr16:2526474..2670331hg18UCSC Ensembl
Outerchr16:2526474..2670331hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38143858
hg19143858
hg18143858
hg17143858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4190, nssv2129, nssv9521
SamplesNA18507, NA12878, NA18555
Known GenesERVK13-1, FLJ42627, LOC652276, PDPK1
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)nsv7275
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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