A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6804



Internal ID15537059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:57795702..57881260hg38UCSC Ensembl
Outerchr19:58307070..58392628hg19UCSC Ensembl
Outerchr19:62998882..63084440hg18UCSC Ensembl
Outerchr19:62998882..63084440hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3885559
hg1985559
hg1885559
hg1785559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7311
Supporting Variants
SamplesNA12156
Known GenesFKBP1AP1, ZNF552, ZNF587, ZNF587B, ZNF814
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)nssv6804
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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