A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373972



Internal ID21031525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165015229..165015981hg38UCSC Ensembl
chr3:164733017..164733769hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097069
Samples
Known GenesSI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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