A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416268



Internal ID22474138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16405916..16631070hg38UCSC Ensembl
chr4:16407539..16632693hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38225155
hg19225155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979278
Supporting Variants
Samples
Known GenesLDB2, MIR548AX
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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