A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037108



Internal ID20604148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61693601..61694100hg38UCSC Ensembl
chr17:59770962..59771461hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529693
Supporting Variants
Samples
Known GenesBRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer