A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581456



Internal ID20954527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37823075..37823677hg38UCSC Ensembl
chr10:38112003..38112605hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228767
Samples
Known GenesZNF248
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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