A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4899n100



Internal ID22790986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130072493..130109235hg38UCSC Ensembl
chr3:129791336..129828078hg19UCSC Ensembl
chr3:131274026..131310768hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3836743
hg1936743
hg1836743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010091, nsv1008270, nsv1001961
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4899n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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