A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3546652



Internal ID18498247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30212863..30488448hg38UCSC Ensembl
Innerchr15:30505066..30780651hg19UCSC Ensembl
Innerchr15:28292358..28567943hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38275586
hg19275586
hg18275586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054072
Supporting Variants
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)nssv3546652
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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