A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351155



Internal ID22576824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177277131..177278391hg38UCSC Ensembl
chr1:177246267..177247527hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886788
Supporting Variants
Samples
Known GenesBRINP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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