A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570662



Internal ID20943733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107828405..107830326hg38UCSC Ensembl
chr4:108749561..108751482hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381922
hg191922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263469
Samples
Known GenesSGMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570662
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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