A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423804



Internal ID21081357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138358789..138361579hg38UCSC Ensembl
chr7:138043534..138046324hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382791
hg192791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155202
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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