A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811262



Internal ID21256600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83692950..83693027hg38UCSC Ensembl
chr4:84614103..84614180hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811262
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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