A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905341



Internal ID4371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6260738..6262525hg38UCSC Ensembl
chr1:6320798..6322585hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433221
Supporting Variants
Samples
Known GenesGPR153
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905341
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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