A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344949



Internal ID21002502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39935491..40079259hg38UCSC Ensembl
chr2:40162631..40306399hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38143769
hg19143769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089760
Samples
Known GenesSLC8A1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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