A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574499



Internal ID20947570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175488036..175906062hg38UCSC Ensembl
chr4:176409187..176827213hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38418027
hg19418027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263918
Samples
Known GenesGPM6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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