A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980499



Internal ID18615699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182372638..182377775hg38UCSC Ensembl
Innerchr4:183293791..183298928hg19UCSC Ensembl
Innerchr4:183530785..183535922hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385138
hg195138
hg185138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758937
SamplesHGDP00456
Known GenesTENM3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980499
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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