A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812354



Internal ID21257692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150372380..150372505hg38UCSC Ensembl
chr6:150693516..150693641hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696542
Samples
Known GenesIYD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812354
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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