A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350324



Internal ID21007877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61845877..61973371hg38UCSC Ensembl
chr2:62073012..62200506hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38127495
hg19127495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206377
Samples
Known GenesCCT4, COMMD1, FAM161A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350324
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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