A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907762



Internal ID22682972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96537677..96539753hg38UCSC Ensembl
chr8:97549905..97551981hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431269
Samples
Known GenesSDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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