A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049860



Internal ID18792391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68083566..68141729hg38UCSC Ensembl
Innerchr15:68375904..68434067hg19UCSC Ensembl
Innerchr15:66162958..66221121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3858164
hg1958164
hg1858164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2615n100
Supporting Variantsnssv3553655
Samples
Known GenesPIAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049860
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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