A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536176



Internal ID20909531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71493190..71493572hg38UCSC Ensembl
chr2:71720320..71720702hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258966
Samples
Known GenesDYSF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536176
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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