A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360422



Internal ID21017975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136812355..136830550hg38UCSC Ensembl
chr3:136531197..136549392hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3818196
hg1918196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094963
Samples
Known GenesSLC35G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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