A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388636



Internal ID21046189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32162967..32195031hg38UCSC Ensembl
chr5:32163073..32195137hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3832065
hg1932065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130915
Samples
Known GenesGOLPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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