A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548252



Internal ID20921448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135967999..135968940hg38UCSC Ensembl
chr2:136725569..136726510hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255926
Samples
Known GenesDARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548252
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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