A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061096



Internal ID20628136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45619012..45624753hg38UCSC Ensembl
chr1:46084684..46090425hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg385742
hg195742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332914
Supporting Variants
Samples
Known GenesCCDC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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