A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544307



Internal ID20917546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76576058..77121996hg38UCSC Ensembl
chr2:76803184..77349122hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38545939
hg19545939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258396
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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