A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136526



Internal ID20703566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95512701..95523500hg38UCSC Ensembl
chr5:94848405..94859204hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399209
Supporting Variants
Samples
Known GenesTTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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