A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343020



Internal ID21000573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:178481691..178484646hg38UCSC Ensembl
chr2:179346418..179349373hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg382956
hg192956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082739
Samples
Known GenesMIR548N, PLEKHA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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