A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577938



Internal ID21526398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51391488..51391803hg38UCSC Ensembl
chr6:51256286..51256601hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152627
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577938
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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