A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391182



Internal ID22449052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35071985..35072582hg38UCSC Ensembl
chr19:35562889..35563486hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978807
Supporting Variants
Samples
Known GenesHPN-AS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391182
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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