A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035518



Internal ID18778049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30297839..30472412hg38UCSC Ensembl
Innerchr15:30590042..30764615hg19UCSC Ensembl
Innerchr15:28377334..28551907hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38174574
hg19174574
hg18174574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2513n100
Supporting Variantsnssv3546711
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035518
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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