A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3517n100



Internal ID22789604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34825081..34887191hg38UCSC Ensembl
chr19:35315985..35378095hg19UCSC Ensembl
chr19:40007825..40069935hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3862111
hg1962111
hg1862111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065593, nsv1062596, nsv1059180
Samples
Known GenesLOC400685
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3517n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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