A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902047



Internal ID2159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37548376..37549436hg38UCSC Ensembl
chr1:38013977..38015037hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381061
hg191061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431338
Supporting Variants
Samples
Known GenesSNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902047
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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