A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426653



Internal ID21084206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146864203..146962783hg38UCSC Ensembl
chr7:146561295..146659875hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3898581
hg1998581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7164n223
Supporting Variantsnssv18155910
Samples
Known GenesCNTNAP2, MIR548AQ, MIR548AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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