A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600591



Internal ID20973662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69633195..69704867hg38UCSC Ensembl
chr7:69098181..69169853hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3871673
hg1971673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160152
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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