A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256171



Internal ID21399811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87925967..87937206hg38UCSC Ensembl
chr4:88847119..88858358hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3811240
hg1911240
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730077
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256171
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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