A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853144



Internal ID22628079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146160987..146162366hg38UCSC Ensembl
chr7:145858079..145859458hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502206
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853144
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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