A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495268



Internal ID22553201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48888068..48890090hg38UCSC Ensembl
chr4:48890085..48892107hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg382023
hg192023
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839053
Supporting Variants
Samples
Known GenesOCIAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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