A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339622



Internal ID20997175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173133901..173144500hg38UCSC Ensembl
chr2:173998629..174009228hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080454
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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