A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884603



Internal ID22659586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7616532..7620637hg38UCSC Ensembl
chr1:7676592..7680697hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384106
hg194106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385655
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884603
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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