A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347277



Internal ID21004830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42511801..42530200hg38UCSC Ensembl
chr2:42738941..42757340hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3818400
hg1918400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087892
Samples
Known GenesMTA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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