A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153262



Internal ID21494789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74759251..74759251hg38UCSC Ensembl
chr5:74055076..74055076hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629465
Supporting Variants
SamplesNA19238
Known GenesGFM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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