A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360040



Internal ID21017593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15307144..15308317hg38UCSC Ensembl
chr3:15348651..15349824hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096770
Samples
Known GenesSH3BP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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