A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3591n100



Internal ID20155207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43138388..43372382hg38UCSC Ensembl
chr19:43642540..43876534hg19UCSC Ensembl
chr19:48334380..48568374hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38233995
hg19233995
hg18233995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056910, nsv1056183, nsv1065023, nsv1057430, nsv1064002, nsv1066677, nsv1063262, nsv1062110, nsv1063723, nsv1060137, nsv1061779, nsv1064467, nsv1056122, nsv1061385, nsv1058727, nsv1060310, nsv1055952, nsv1061772, nsv1062704, nsv1061582, nsv1063021, nsv1056421, nsv1060224
Samples
Known GenesCD177, LOC284344, PRG1, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3591n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss111
Observed Complex0
Frequencyn/a


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