A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344855



Internal ID21002408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61066501..61070100hg38UCSC Ensembl
chr2:61293636..61297235hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206367
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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