A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334324



Internal ID20867508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107517901..107531300hg38UCSC Ensembl
chr1:108060523..108073922hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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