A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365934



Internal ID21023487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16076570..16077643hg38UCSC Ensembl
chr4:16078193..16079266hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113013
Samples
Known GenesPROM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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