A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364801



Internal ID21022354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47595779..47597354hg38UCSC Ensembl
chr3:47637269..47638844hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381576
hg191576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100768
Samples
Known GenesSMARCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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