A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812238



Internal ID21257576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177517608..177518330hg38UCSC Ensembl
chr5:176944609..176945331hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812238
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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