A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331738



Internal ID20864904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103423116..103423593hg38UCSC Ensembl
chr1:103965738..103966215hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050211
Samples
Known GenesLOC101928436
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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