A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434899



Internal ID21396901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27807223..27839222hg38UCSC Ensembl
chr6:27775001..27807000hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3832000
hg1932000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750301
SamplesSMI041
Known GenesHIST1H2AI, HIST1H2AJ, HIST1H2AK, HIST1H2BL, HIST1H2BM, HIST1H2BN, HIST1H3H, HIST1H4J, HIST1H4K
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434899
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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