A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341623



Internal ID20999176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178909015..179011805hg38UCSC Ensembl
chr2:179773742..179876532hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38102791
hg19102791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082766
Samples
Known GenesCCDC141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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