A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573786



Internal ID18872067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44392222..44434102hg38UCSC Ensembl
Innerchr19:44896386..44938277hg19UCSC Ensembl
Innerchr19:49588226..49630117hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3841881
hg1941892
hg1841892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059267
Supporting Variants
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573786
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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