A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055357



Internal ID18797888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56422263..56678639hg38UCSC Ensembl
Innerchr19:56933632..57190007hg19UCSC Ensembl
Innerchr19:61625444..61881819hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38256377
hg19256376
hg18256376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726647
Samples
Known GenesSMIM17, ZFP28, ZNF470, ZNF471, ZNF583, ZNF667, ZNF667-AS1, ZNF71, ZNF835
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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