A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557529



Internal ID20930600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37606869..37609109hg38UCSC Ensembl
chr5:37606971..37609211hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268303
Samples
Known GenesWDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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