A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509876



Internal ID20883189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31960667..31964324hg38UCSC Ensembl
chr17:30287686..30291343hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383658
hg193658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034924
Samples
Known GenesSUZ12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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