A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098567



Internal ID21456298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6820694..6820694hg38UCSC Ensembl
chr12:6929860..6929860hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg384524
hg194524
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660561
Supporting Variants
SamplesHG02492
Known GenesCD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098567
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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