A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527529



Internal ID20900890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78193384..78198774hg38UCSC Ensembl
chr17:76189465..76194855hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385391
hg195391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038083
Samples
Known GenesAFMID
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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