A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334689



Internal ID20867876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160877101..160881700hg38UCSC Ensembl
chr1:160846891..160851490hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052476
Samples
Known GenesITLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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