A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911753



Internal ID22686968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26247770..26247866hg38UCSC Ensembl
chr10:26536699..26536795hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367082
Samples
Known GenesGAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911753
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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