A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584014



Internal ID20957085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25058223..25058931hg38UCSC Ensembl
chr10:25347152..25347860hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv656n223
Supporting Variantsnssv18228542
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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