A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571500



Internal ID21519880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90527856..90528176hg38UCSC Ensembl
chr6:91237575..91237895hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150747
SamplesHG00731
Known GenesMAP3K7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571500
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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