A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359957



Internal ID21017510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120179501..120202500hg38UCSC Ensembl
chr3:119898348..119921347hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3823000
hg1923000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093573
Samples
Known GenesGPR156
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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