A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420227



Internal ID21077780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146320164..146339913hg38UCSC Ensembl
chr7:146017256..146037005hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3819750
hg1919750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155817
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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