A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539365



Internal ID20912663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47472792..47473298hg38UCSC Ensembl
chr2:47699931..47700437hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258051
Samples
Known GenesMSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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