A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351090



Internal ID21008643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214415379..214415825hg38UCSC Ensembl
chr2:215280103..215280549hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083406
Samples
Known GenesVWC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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