A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041607



Internal ID19130826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26353403..26376082hg38UCSC Ensembl
Innerchr15:26598550..26621229hg19UCSC Ensembl
Innerchr15:24149643..24172322hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3822680
hg1922680
hg1822680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545633
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041607
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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