A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3575001



Internal ID18873282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51628371..51654150hg38UCSC Ensembl
Innerchr19:52131624..52157403hg19UCSC Ensembl
Innerchr19:56823436..56849215hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3825780
hg1925780
hg1825780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064047
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)nssv3575001
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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