A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636906



Internal ID7023700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74600669..74604335hg38UCSC Ensembl
Innerchr15:74600669..74604335hg38UCSC Ensembl
Outerchr15:74600370..74604548hg38UCSC Ensembl
chr15:74893010..74896676hg19UCSC Ensembl
Innerchr15:74893010..74896676hg19UCSC Ensembl
Outerchr15:74892711..74896889hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292822, essv15292817, essv15292824, essv15292818, essv15292819, essv15292823, essv15292815, essv15292814, essv15292816, essv15292821, essv15292820, essv15292825
SamplesHG03095, HG03385, NA19024, HG02582, HG03388, HG03451, HG02308, HG03419, HG03084, NA19438, NA18876, NA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636906
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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