A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054724



Internal ID19143943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90283720..90313106hg38UCSC Ensembl
Innerchr15:90826952..90856338hg19UCSC Ensembl
Innerchr15:88627956..88657342hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3829387
hg1929387
hg1829387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2657n100
Supporting Variantsnssv3555200, nssv3555199, nssv3718189
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)nsv1054724
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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