A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351123



Internal ID21008676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214788266..214789009hg38UCSC Ensembl
chr2:215652990..215653733hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083441
Samples
Known GenesBARD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351123
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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