A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960798



Internal ID18866548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:22385808..22671023hg38UCSC Ensembl
Outerchr19:22568610..22853825hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38285216
hg19285216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120056
Supporting Variants
SamplesKWS1
Known GenesLOC100996349, LOC440518, ZNF492, ZNF98
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960798
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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