A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3623n100



Internal ID22789710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51623777..51655602hg38UCSC Ensembl
chr19:52127030..52158855hg19UCSC Ensembl
chr19:56818842..56850667hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3831826
hg1931826
hg1831826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064047, nsv1056104, nsv1062399, nsv1057374, nsv1055268
Samples
Known GenesSIGLEC14, SIGLEC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3623n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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