A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573754



Internal ID20946825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87341216..87341605hg38UCSC Ensembl
chr4:88262368..88262757hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266713
Samples
Known GenesHSD17B11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573754
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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