A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320102



Internal ID20853200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218850701..218855800hg38UCSC Ensembl
chr1:219024043..219029142hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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