A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812255



Internal ID21257593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178793844..178793915hg38UCSC Ensembl
chr5:178220845..178220916hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812255
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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