A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048726



Internal ID19137945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48927755..48948761hg38UCSC Ensembl
Innerchr15:49219952..49240958hg19UCSC Ensembl
Innerchr15:47007244..47028250hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3821007
hg1921007
hg1821007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552380
Samples
Known GenesSHC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048726
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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