A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972461



Internal ID22747396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101995734..102278551hg38UCSC Ensembl
chr4:102916891..103199708hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38282818
hg19282818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419200
Samples
Known GenesBANK1, SLC39A8
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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