A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584927



Internal ID20957998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73145111..73145912hg38UCSC Ensembl
chr10:74904869..74905670hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217528
Samples
Known GenesECD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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