A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399194



Internal ID21056747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65992905..65994744hg38UCSC Ensembl
chr5:65288733..65290572hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133265
Samples
Known GenesERBB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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