A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409431



Internal ID21066984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65677986..65683361hg38UCSC Ensembl
chr5:64973813..64979188hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385376
hg195376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133248
Samples
Known GenesSGTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409431
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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