A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461278



Internal ID22519161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88284919..88303303hg38UCSC Ensembl
chr13:88937174..88955558hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3818385
hg1918385
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461278
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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