A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850367



Internal ID22625302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147166279..147175417hg38UCSC Ensembl
chr7:146863371..146872509hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg389139
hg199139
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502593
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850367
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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