A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501470



Internal ID22559408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65920626..65923340hg38UCSC Ensembl
chr7:65385613..65388327hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382715
hg192715
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854770
Supporting Variants
Samples
Known GenesVKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501470
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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