A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543142



Internal ID20916393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10154428..10154507hg38UCSC Ensembl
chr2:10294555..10294634hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255737
Samples
Known GenesC2orf48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543142
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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