A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149471



Internal ID21457020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65891354..65896898hg38UCSC Ensembl
chr7:65356341..65361885hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385545
hg195545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569865
Supporting Variants
SamplesHG02587
Known GenesVKORC1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149471
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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