A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331581



Internal ID20864745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217179384..217180057hg38UCSC Ensembl
chr1:217352726..217353399hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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