A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040915



Internal ID19130134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24819264..24850892hg38UCSC Ensembl
Innerchr15:25064411..25096039hg19UCSC Ensembl
Innerchr15:22615504..22647132hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3831629
hg1931629
hg1831629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2471n100
Supporting Variantsnssv3545380
Samples
Known GenesSNRPN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040915
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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