A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399198



Internal ID21056751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156655467..156656084hg38UCSC Ensembl
chr5:156082478..156083095hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127697
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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