A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333151



Internal ID20866327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173836491..173841287hg38UCSC Ensembl
chr1:173805629..173810425hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg384797
hg194797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053145
Samples
Known GenesDARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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