A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043423



Internal ID18785954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71112552..71337743hg38UCSC Ensembl
Innerchr15:71404891..71630082hg19UCSC Ensembl
Innerchr15:69191945..69417136hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38225192
hg19225192
hg18225192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553685
Samples
Known GenesCT62, THSD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043423
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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