A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432485



Internal ID21394487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21290689..21450688hg38UCSC Ensembl
chr17:21194001..21354000hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38160000
hg19160000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv310n172
Supporting Variantsnssv15746398, nssv15751750, nssv15747020, nssv15754098, nssv15751803, nssv15748107, nssv15748788
SamplesNB08, BTQ038, NB10, BTQ055, MDQ010, BTQ016, NB11
Known GenesKCNJ12, KCNJ18, MAP2K3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432485
Frequency
Sample Size15
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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