A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337872



Internal ID20995425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63486786..63487234hg38UCSC Ensembl
chr2:63713920..63714368hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089241
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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