A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909256



Internal ID22684466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26331769..26344208hg38UCSC Ensembl
chr7:26371389..26383828hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3812440
hg1912440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436814
Samples
Known GenesSNX10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909256
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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