A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349724



Internal ID21007277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62686044..62686667hg38UCSC Ensembl
chr2:62913179..62913802hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089177
Samples
Known GenesEHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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