A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10178



Internal ID15195934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21613099..22060693hg38UCSC Ensembl
Outerchr19:21795901..22243495hg19UCSC Ensembl
Outerchr19:21587741..22035335hg18UCSC Ensembl
Outerchr19:21587741..22035335hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38447595
hg19447595
hg18447595
hg17447595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7306
Supporting Variants
SamplesNA18956
Known GenesLOC641367, ZNF100, ZNF208, ZNF257, ZNF43
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)nssv10178
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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