A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554990



Internal ID20928079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60869878..60870146hg38UCSC Ensembl
chr2:61097013..61097281hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257668
Samples
Known GenesFLJ16341
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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