A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877646



Internal ID22652610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155918602..155918730hg38UCSC Ensembl
chr1:155888393..155888521hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354286
Samples
Known GenesKIAA0907
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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