A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037740



Internal ID20604780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63911373..63918921hg38UCSC Ensembl
chr17:61988733..61996281hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg387549
hg197549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524440
Supporting Variants
Samples
Known GenesGH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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