A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575558



Internal ID20948629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146170146..146170827hg38UCSC Ensembl
chr7:145867238..145867919hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275160
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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