A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152610



Internal ID20719650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126676827..126685277hg38UCSC Ensembl
chr7:126316881..126325331hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg388451
hg198451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435552
Supporting Variants
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152610
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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