A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812394



Internal ID21257732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266088..16266162hg38UCSC Ensembl
chr6:16266319..16266393hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710854
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812394
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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