A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435759



Internal ID21397761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70037085..70039084hg38UCSC Ensembl
chr9:72652001..72654000hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750215, nssv15747451, nssv15745708, nssv15750589, nssv15751482, nssv15754045
SamplesNB12, NB08, NB10, BTQ055, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435759
Frequency
Sample Size15
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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