A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435637



Internal ID21397639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129443721hg38UCSC Ensembl
chr9:132187001..132206000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv864n172
Supporting Variantsnssv15754362, nssv15754598, nssv15745860, nssv15754535, nssv15749227
SamplesNB12, BTQ038, MDQ010, NB11, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435637
Frequency
Sample Size15
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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