A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560897



Internal ID20933968
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 StatusM
Merged Variants
Supporting Variantsnssv18260308
Samples
Known GenesMSL2, PCCB, SLC35G2, STAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560897
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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