A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895084



Internal ID22670161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156449173..156454965hg38UCSC Ensembl
chr5:155876183..155881975hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg385793
hg195793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424265
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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