A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978962



Internal ID18884642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21238778..21410503hg38UCSC Ensembl
Outerchr19:21421580..21593305hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38171726
hg19171726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140249
Supporting Variants
SamplesKWS2
Known GenesZNF493, ZNF708, ZNF738
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978962
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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