A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551192



Internal ID20924329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61024039..61024672hg38UCSC Ensembl
chr2:61251174..61251807hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3897n223
Supporting Variantsnssv18257677
Samples
Known GenesPEX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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