A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812211



Internal ID21257549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168967427..168967739hg38UCSC Ensembl
chr5:168394432..168394744hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701301
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812211
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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