A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154038



Internal ID20721078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149485851..149489497hg38UCSC Ensembl
chr7:149182942..149186588hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383647
hg193647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424243
Supporting Variants
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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