A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337903



Internal ID20995456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10348207..10370359hg38UCSC Ensembl
chr2:10488333..10510485hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3822153
hg1922153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075186
Samples
Known GenesHPCAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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