A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155795



Internal ID20722835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146100824..146744149hg38UCSC Ensembl
chr7:145797916..146441241hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38643326
hg19643326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426801
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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