A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756804



Internal ID20532664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38771816..38790753hg38UCSC Ensembl
chr19:39262456..39281393hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv52n199
Supporting Variantsnssv16280956
Samples
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756804
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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