A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141514



Internal ID20708554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15174503..15179277hg38UCSC Ensembl
chr6:15174734..15179508hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384775
hg194775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0015


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