A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339337



Internal ID20996890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205683630..205688188hg38UCSC Ensembl
chr2:206548354..206552912hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg384559
hg194559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082925
Samples
Known GenesNRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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