A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349716



Internal ID21007269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70070759..70081392hg38UCSC Ensembl
chr2:70297891..70308524hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3810634
hg1910634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088917
Samples
Known GenesPCBP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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