A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967866



Internal ID22742801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3735157..3786600hg38UCSC Ensembl
chr4:3736884..3788327hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3851444
hg1951444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414263
Samples
Known GenesADRA2C
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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