A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352564



Internal ID21010117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77009144..77080521hg38UCSC Ensembl
chr2:77236270..77307647hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3871378
hg1971378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090624
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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