A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613185



Internal ID20986256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23296751..23299337hg38UCSC Ensembl
chr7:23336370..23338956hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382587
hg192587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154911
Samples
Known GenesMALSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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