A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435616



Internal ID21397618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128130722..128138721hg38UCSC Ensembl
chr9:130893001..130901000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746661, nssv15750253, nssv15747992, nssv15754029, nssv15752235, nssv15753505, nssv15748583, nssv15749746, nssv15746880, nssv15745658, nssv15753792, nssv15750189, nssv15751786, nssv15749362, nssv15748440
SamplesNB12, SMI034, NB08, MDQ045, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, NB07, SMI018, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435616
Frequency
Sample Size15
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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