A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463728



Internal ID22521613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33977882..33997808hg38UCSC Ensembl
chr1:34443483..34463409hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3819927
hg1919927
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829701
Supporting Variants
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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