A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416564



Internal ID21074117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147675016..147675528hg38UCSC Ensembl
chr7:147372108..147372620hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153905
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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