A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419578



Internal ID21077131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147802928..147807908hg38UCSC Ensembl
chr7:147500020..147505000hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384981
hg194981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153921
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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