A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347721



Internal ID21005274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201639201..201645900hg38UCSC Ensembl
chr2:202503924..202510623hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208294
Samples
Known GenesMPP4, TMEM237
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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