A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362671



Internal ID21020224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33782612..33783068hg38UCSC Ensembl
chr4:33784234..33784690hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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