A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337041



Internal ID20994594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71062502..71076790hg38UCSC Ensembl
chr2:71289632..71303920hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3814289
hg1914289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089586
Samples
Known GenesNAGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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