A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409439



Internal ID22467309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3541580..3542233hg38UCSC Ensembl
chr19:3541578..3542231hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974095
Supporting Variants
Samples
Known GenesC19orf71, MFSD12
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409439
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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