A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226608



Internal ID20793648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97006001..97007400hg38UCSC Ensembl
chr7:96635313..96636712hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601851
Supporting Variants
Samples
Known GenesDLX6, DLX6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00017


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