A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987806



Internal ID19212754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:23379883..23799875hg38UCSC Ensembl
Outerchr19:23562685..23982677hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38419993
hg19419993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133009
Supporting Variants
SamplesKWS1
Known GenesRPSAP58, ZNF675, ZNF681, ZNF91
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987806
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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