A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356496



Internal ID21014049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155167069..155167727hg38UCSC Ensembl
chr3:154884858..154885516hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096403
Samples
Known GenesMME
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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