A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432526



Internal ID21394528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43226954..43305638hg38UCSC Ensembl
chr17:41379001..41383000hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3878685
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv317n172
Supporting Variantsnssv15752911, nssv15754483, nssv15754213, nssv15751035, nssv15752681, nssv15748731, nssv15754090, nssv15749777, nssv15746749, nssv15750249, nssv15750553, nssv15748948, nssv15748634
SamplesNB12, SMI034, NB08, MDQ045, BTQ038, NB10, BTQ055, MDQ010, BTQ016, NB11, NB07, MDQ025, NB09
Known GenesLINC00854
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432526
Frequency
Sample Size15
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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