A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584330



Internal ID20957401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21341076..21341784hg38UCSC Ensembl
chr10:21630005..21630713hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv644n223
Supporting Variantsnssv18229214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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