A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542995



Internal ID20916246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210977463..210995631hg38UCSC Ensembl
chr2:211842187..211860355hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3818169
hg1918169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542995
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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