A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570435



Internal ID18522030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:55754298..55789134hg38UCSC Ensembl
Innerchr19:56265664..56300500hg19UCSC Ensembl
Innerchr19:60957476..60992312hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3834837
hg1934837
hg1834837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066324
Supporting Variants
Samples
Known GenesNLRP11, RFPL4A, RFPL4AL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3570435
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