A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351631



Internal ID21009184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157269685..157270175hg38UCSC Ensembl
chr2:158126197..158126687hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079785
Samples
Known GenesGALNT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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