A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895731



Internal ID15843001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17259381..17285740hg38UCSC Ensembl
Innerchr19:17370190..17396549hg19UCSC Ensembl
Innerchr19:17231190..17257549hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3826360
hg1926360
hg1826360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578740
Supporting Variants
Samples
Known GenesANKLE1, BABAM1, USHBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895731
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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