A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409173



Internal ID21066726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156717803..156718934hg38UCSC Ensembl
chr5:156144814..156145945hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127706
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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