A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344298



Internal ID21001851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180875417..180914229hg38UCSC Ensembl
chr2:181740144..181778956hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3838813
hg1938813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081119
Samples
Known GenesSCHLAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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