A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053692



Internal ID18796223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30439291hg38UCSC Ensembl
Innerchr15:30505066..30731494hg19UCSC Ensembl
Innerchr15:28292358..28518786hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38226429
hg19226429
hg18226429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2507n100
Supporting Variantsnssv3546649
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053692
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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