A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531182



Internal ID20904543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77094288..77100640hg38UCSC Ensembl
chr17:75090370..75096722hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg386353
hg196353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037737
Samples
Known GenesLINC00338, SEC14L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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