A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570597



Internal ID20943668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75971563..75972260hg38UCSC Ensembl
chr4:76892716..76893413hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264692
Samples
Known GenesSDAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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