A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7306



Internal ID15205616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21613099..22098259hg38UCSC Ensembl
Outerchr19:21795901..22281061hg19UCSC Ensembl
Outerchr19:21587741..22072901hg18UCSC Ensembl
Outerchr19:21587741..22072901hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38485161
hg19485161
hg18485161
hg17485161
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10179, nssv10178
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)nsv7306
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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