A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10179



Internal ID15195933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21649930..22098259hg38UCSC Ensembl
Outerchr19:21832732..22281061hg19UCSC Ensembl
Outerchr19:21624572..22072901hg18UCSC Ensembl
Outerchr19:21624572..22072901hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38448330
hg19448330
hg18448330
hg17448330
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
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)nssv10179
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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