A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569825



Internal ID16357234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183376..71185482hg38UCSC Ensembl
Innerchr15:71475715..71477821hg19UCSC Ensembl
Innerchr15:69262769..69264875hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382107
hg192107
hg182107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4587n54
Supporting Variantsnssv844388, nssv844384, nssv844389, nssv844391, nssv844385, nssv844387, nssv844390, nssv844392, nssv844386
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569825
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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