A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331103



Internal ID20864264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168646333..168646564hg38UCSC Ensembl
chr1:168615571..168615802hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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