A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058846



Internal ID19148065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33009355..33060155hg38UCSC Ensembl
Innerchr19:33500261..33551061hg19UCSC Ensembl
Innerchr19:38192101..38242901hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3850801
hg1950801
hg1850801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566576
Samples
Known GenesRHPN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058846
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