A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812643



Internal ID21257981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108031342..108031443hg38UCSC Ensembl
chr6:108352546..108352647hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812643
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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