A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612672



Internal ID20985743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111800116..111800882hg38UCSC Ensembl
chr6:112121319..112122085hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135428
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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