A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3435221



Internal ID15282175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30375157..30376455hg38UCSC Ensembl
Innerchr15:30375455..30376157hg38UCSC Ensembl
Outerchr15:30374157..30377455hg38UCSC Ensembl
chr15:30667360..30668658hg19UCSC Ensembl
Innerchr15:30667658..30668360hg19UCSC Ensembl
Outerchr15:30666360..30669658hg19UCSC Ensembl
chr15:28454652..28455950hg18UCSC Ensembl
Innerchr15:28455652..28454950hg18UCSC Ensembl
Outerchr15:28453652..28456950hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1399e59
Supporting Variantsessv8689760
SamplesNA19240
Known GenesCHRFAM7A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3435221
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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