A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341952



Internal ID20999505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:106155609..106156064hg38UCSC Ensembl
chr2:106772065..106772520hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076666
Samples
Known GenesUXS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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