A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924049



Internal ID22699276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22947247..22960254hg38UCSC Ensembl
chr7:22986866..22999873hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3813008
hg1913008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445159
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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