A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416224



Internal ID22474094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158500774..158878861hg38UCSC Ensembl
chr4:159421926..159800013hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38378088
hg19378088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973186
Supporting Variants
Samples
Known GenesC4orf46, ETFDH, FNIP2, PPID, RXFP1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416224
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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