A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3575002



Internal ID18873283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51628371..51654172hg38UCSC Ensembl
Innerchr19:52131624..52157425hg19UCSC Ensembl
Innerchr19:56823436..56849237hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3825802
hg1925802
hg1825802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062399
Supporting Variants
Samples
Known GenesSIGLEC14, SIGLEC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3575002
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