A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050357



Internal ID18792888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313356..30440064hg38UCSC Ensembl
Innerchr15:30605559..30732267hg19UCSC Ensembl
Innerchr15:28392851..28519559hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38126709
hg19126709
hg18126709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2512n100
Supporting Variantsnssv3546747
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)nsv1050357
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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