A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401366



Internal ID22459236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52690058..53366131hg38UCSC Ensembl
chr19:53193311..53869384hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38676074
hg19676074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978948
Supporting Variants
Samples
Known GenesBIRC8, ERVV-1, ERVV-2, FAM90A27P, VN1R2, VN1R4, ZNF160, ZNF28, ZNF320, ZNF321P, ZNF347, ZNF415, ZNF468, ZNF525, ZNF600, ZNF611, ZNF665, ZNF677, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF818P, ZNF83, ZNF845
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401366
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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