A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573770



Internal ID18872051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43380906..43431018hg38UCSC Ensembl
Innerchr19:43885058..43935170hg19UCSC Ensembl
Innerchr19:48576898..48627010hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3850113
hg1950113
hg1850113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057949
Supporting Variants
Samples
Known GenesTEX101
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573770
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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