A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3524n100



Internal ID20155140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36315573..36362200hg38UCSC Ensembl
chr19:36806475..36853102hg19UCSC Ensembl
chr19:41498315..41544942hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3846628
hg1946628
hg1846628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059568, nsv1064343
Samples
Known GenesLINC00665, ZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3524n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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