A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065923



Internal ID18808454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..30015920hg38UCSC Ensembl
Innerchr19:30455280..30506827hg19UCSC Ensembl
Innerchr19:35147120..35198667hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3851548
hg1951548
hg1851548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3510n100
Supporting Variantsnssv3566546, nssv3566547
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065923
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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