A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709037



Internal ID21198390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38769343..38782967hg38UCSC Ensembl
chr19:39259983..39273607hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3813625
hg1913625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799997
Supporting Variants
SamplesCHM1
Known GenesLGALS7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709037
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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