A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336571



Internal ID20994124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112023582..112024063hg38UCSC Ensembl
chr2:112781159..112781640hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075556
Samples
Known GenesMERTK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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