A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545164



Internal ID20918396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178847621..179451406hg38UCSC Ensembl
chr2:179712348..180316133hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38603786
hg19603786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256301
Samples
Known GenesCCDC141, SESTD1, ZNF385B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545164
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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