A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799997



Internal ID21245337
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 StatusM
Merged Variants
Supporting Variantsnssv13709037
SamplesCHM1
Known GenesLGALS7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799997
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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