A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609605



Internal ID20982676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70566484..70566871hg38UCSC Ensembl
chr7:70031470..70031857hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158664
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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