A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155032



Internal ID20722072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24724410..24728839hg38UCSC Ensembl
chr7:24764029..24768458hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg384430
hg194430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618112
Supporting Variants
Samples
Known GenesDFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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