A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150099



Internal ID20717139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123705601..123707600hg38UCSC Ensembl
chr7:123345655..123347654hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613412
Supporting Variants
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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