A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355907



Internal ID22581576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202942217..202943755hg38UCSC Ensembl
chr1:202911345..202912883hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381539
hg191539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867671
Supporting Variants
Samples
Known GenesADIPOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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