A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582177



Internal ID20955248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100111005..100111659hg38UCSC Ensembl
chr10:101870762..101871416hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582177
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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