A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572778



Internal ID20945849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172767336..172767936hg38UCSC Ensembl
chr3:172485126..172485726hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259880
Samples
Known GenesECT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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