A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260308



Internal ID20827348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136184622..136819803hg38UCSC Ensembl
chr3:135903464..136538645hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38635182
hg19635182
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560897
Supporting Variants
Samples
Known GenesMSL2, PCCB, SLC35G2, STAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260308
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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