A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616998



Internal ID20990069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70445986..70452701hg38UCSC Ensembl
chr7:69910972..69917687hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg386716
hg196716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158657
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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