A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547649



Internal ID20920850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42592994..42594235hg38UCSC Ensembl
chr2:42820134..42821375hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257939
Samples
Known GenesMTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547649
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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