A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340888



Internal ID20998441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100106143..100167932hg38UCSC Ensembl
chr2:100722605..100784394hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3861790
hg1961790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074653
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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