A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345695



Internal ID21003248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176151462..176156434hg38UCSC Ensembl
chr2:177016190..177021162hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg384973
hg194973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082034
Samples
Known GenesHOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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