A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349100



Internal ID21006653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68365996..68372552hg38UCSC Ensembl
chr2:68593128..68599684hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg386557
hg196557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088831
Samples
Known GenesPLEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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