A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507119



Internal ID20880407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16442720..16443447hg38UCSC Ensembl
chr17:16346034..16346761hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034617
Samples
Known GenesFAM211A, FAM211A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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