A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145419



Internal ID21464992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1897923..1898046hg38UCSC Ensembl
chr6:1898157..1898280hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565409
Supporting Variants
SamplesHG03065
Known GenesGMDS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145419
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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