A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3523n100



Internal ID20155139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36252559..36356920hg38UCSC Ensembl
chr19:36743461..36847822hg19UCSC Ensembl
chr19:41435301..41539662hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38104362
hg19104362
hg18104362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056901, nsv1064983, nsv1057579, nsv1055260, nsv1056850, nsv1061054, nsv1063208
Samples
Known GenesLINC00665, LOC100134317, ZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3523n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer