A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364104



Internal ID21021657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112943143..112943899hg38UCSC Ensembl
chr3:112661990..112662746hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093117
Samples
Known GenesCD200R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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