A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333684



Internal ID20866864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153520044..153539226hg38UCSC Ensembl
chr1:153492520..153511702hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3819183
hg1919183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051982
Samples
Known GenesS100A5, S100A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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