A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572205



Internal ID21520591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7741381..7741516hg38UCSC Ensembl
chr6:7741614..7741749hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157206
SamplesNA19239
Known GenesBMP6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572205
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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