A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341569



Internal ID20999122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68040301..68042500hg38UCSC Ensembl
chr2:68267433..68269632hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088814
Samples
Known GenesC1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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