A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545633



Internal ID18843914
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 StatusS
Merged Variantsnsv1041607
Supporting Variants
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)nssv3545633
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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