A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340930



Internal ID20998483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44383271..44398828hg38UCSC Ensembl
chr2:44610410..44625967hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3815558
hg1915558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088643
Samples
Known GenesCAMKMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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