A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151475



Internal ID21423953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142043242..142043590hg38UCSC Ensembl
chr7:141743042..141743390hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574713
Supporting Variants
SamplesHG00731
Known GenesMGAM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151475
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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