A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145328



Internal ID20712368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83223723..83226789hg38UCSC Ensembl
chr6:83933442..83936508hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg383067
hg193067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402444
Supporting Variants
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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