A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348506



Internal ID21006059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181909510..181910354hg38UCSC Ensembl
chr2:182774237..182775081hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080988
Samples
Known GenesSSFA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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