A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336685



Internal ID20994238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85707578..85710881hg38UCSC Ensembl
chr2:85934701..85938004hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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