A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538538



Internal ID20911852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173850675..173851067hg38UCSC Ensembl
chr1:173819813..173820205hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248706
Samples
Known GenesDARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538538
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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