A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417634



Internal ID22475504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72480203..72490776hg38UCSC Ensembl
chr5:71776030..71786603hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3810574
hg1910574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974581
Supporting Variants
Samples
Known GenesZNF366
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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