A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333078



Internal ID20866253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235552976..235564895hg38UCSC Ensembl
chr1:235716276..235728195hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3811920
hg1911920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058872
Samples
Known GenesGNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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