A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5336n100



Internal ID22791423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89910654..90031572hg38UCSC Ensembl
chr4:90831805..90952723hg19UCSC Ensembl
chr4:91050828..91171746hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38120919
hg19120919
hg18120919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003903, nsv999030, nsv998230, nsv1011876
Samples
Known GenesMMRN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5336n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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