A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345929



Internal ID21003482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172237841..172243720hg38UCSC Ensembl
chr2:173102569..173108448hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg385880
hg195880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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