A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585908



Internal ID20958979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101909005..101909216hg38UCSC Ensembl
chr10:103668762..103668973hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228211
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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