A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978963



Internal ID19237187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:23379881..23799828hg38UCSC Ensembl
Outerchr19:23562683..23982630hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38419948
hg19419948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140250
Supporting Variants
SamplesKWS2
Known GenesRPSAP58, ZNF675, ZNF681, ZNF91
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978963
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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