A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148144



Internal ID21422565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7221815..7222134hg38UCSC Ensembl
chr5:7221928..7222247hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566889
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148144
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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