A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895743



Internal ID22670829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151751774..151751980hg38UCSC Ensembl
chr6:152072909..152073115hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429559
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895743
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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