A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765093



Internal ID18963157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22404505..22652146hg38UCSC Ensembl
chr19:22587307..22834948hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38247642
hg19247642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078307
Supporting Variants
SamplesKWP1
Known GenesLOC100996349, LOC440518, ZNF492, ZNF98
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765093
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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