A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142772



Internal ID21471213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137946924..137946924hg38UCSC Ensembl
chr7:137631670..137631670hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640185
Supporting Variants
SamplesHG03125
Known GenesCREB3L2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142772
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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