A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460876



Internal ID21118429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70609849..70613046hg38UCSC Ensembl
chr11:70455954..70459151hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383198
hg193198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992836
Samples
Known GenesSHANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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