A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4190



Internal ID15192231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2559306..2680329hg38UCSC Ensembl
Outerchr16:2609307..2730330hg19UCSC Ensembl
Outerchr16:2549308..2670331hg18UCSC Ensembl
Outerchr16:2549308..2670331hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38121024
hg19121024
hg18121024
hg17121024
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7275
Supporting Variants
SamplesNA12878
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)nssv4190
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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