A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915802



Internal ID22691020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4956818..6213781hg38UCSC Ensembl
chr9:4956818..6213781hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381256964
hg191256964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434711
Samples
Known GenesCD274, ERMP1, INSL4, INSL6, JAK2, KIAA1432, KIAA2026, MIR4665, MLANA, PDCD1LG2, PLGRKT, RANBP6, RLN1, RLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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