A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572932



Internal ID20946003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136832220..136832837hg38UCSC Ensembl
chr3:136551062..136551679hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259685
Samples
Known GenesSLC35G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572932
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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