A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434783



Internal ID21396785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153420866..153430865hg38UCSC Ensembl
chr6:153742001..153752000hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv720n172
Supporting Variantsnssv15752814, nssv15747999, nssv15753665, nssv15751029, nssv15748361, nssv15754122, nssv15748982, nssv15749974, nssv15750598
SamplesNB08, MDQ045, BTQ055, BTQ016, SMI041, NB11, NB07, SMI018, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434783
Frequency
Sample Size15
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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