A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590560



Internal ID20963631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74273768..74274269hg38UCSC Ensembl
chr10:76033526..76034027hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814n223
Supporting Variantsnssv18228610
Samples
Known GenesADK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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