A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383162



Internal ID22441032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60717755..60718274hg38UCSC Ensembl
chr1:61183427..61183946hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879495
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383162
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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