A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636868



Internal ID7023662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71996586..71999332hg38UCSC Ensembl
Innerchr15:71996586..71999332hg38UCSC Ensembl
Outerchr15:71996358..71999573hg38UCSC Ensembl
chr15:72288927..72291673hg19UCSC Ensembl
Innerchr15:72288927..72291673hg19UCSC Ensembl
Outerchr15:72288699..72291914hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382747
hg192747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15287975, essv15287972, essv15287973, essv15287977, essv15287976, essv15287978, essv15287971, essv15287974
SamplesHG02891, HG03095, HG03436, HG03224, NA18867, HG03060, HG03445, HG02284
Known GenesMYO9A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636868
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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