A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331220



Internal ID20864382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153451793..153458513hg38UCSC Ensembl
chr1:153424269..153430989hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg386721
hg196721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051980
Samples
Known GenesS100A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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