A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349410



Internal ID21006963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213718284..213721773hg38UCSC Ensembl
chr2:214583008..214586497hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg383490
hg193490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083657
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349410
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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