A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578604



Internal ID16366013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9168223..9175919hg38UCSC Ensembl
Innerchr19:9278899..9286595hg19UCSC Ensembl
Innerchr19:9139899..9147595hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387697
hg197697
hg187697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6263n54
Supporting Variantsnssv893537
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578604
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