A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037007



Internal ID20604047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56472171..56472609hg38UCSC Ensembl
chr17:54549532..54549970hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529644
Supporting Variants
Samples
Known GenesANKFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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