A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146821



Internal ID20713861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93416601..93417200hg38UCSC Ensembl
chr6:94126319..94126918hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405687
Supporting Variants
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00494


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