A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847304



Internal ID22622239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:48675546..48686732hg38UCSC Ensembl
chr7:48715142..48726328hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3811187
hg1911187
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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