A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401638



Internal ID21059191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65676840..65677804hg38UCSC Ensembl
chr5:64972667..64973631hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133247
Samples
Known GenesSGTB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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