A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572544



Internal ID21520935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149027643..149027725hg38UCSC Ensembl
chr7:148724735..148724817hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157878
SamplesHG03371
Known GenesPDIA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572544
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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