A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356353



Internal ID21013906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30922113..30941306hg38UCSC Ensembl
chr4:30923735..30942928hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3819194
hg1919194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214662
Samples
Known GenesPCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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