A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542743



Internal ID20916001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173875711..173876311hg38UCSC Ensembl
chr2:174740439..174741039hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542743
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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