A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402003



Internal ID21059556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169551101..169552700hg38UCSC Ensembl
chr5:168978105..168979704hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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