A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999537



Internal ID19192088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52549807..52773245hg38UCSC Ensembl
Outerchr19:53053060..53276498hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38223439
hg19223439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146332
Supporting Variants
SamplesKWB1
Known GenesZNF137P, ZNF600, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999537
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer