A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572291



Internal ID20945362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175732219..175733328hg38UCSC Ensembl
chr4:176653370..176654479hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263923
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572291
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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