A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2519131



Internal ID8582689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20277163..20280769hg38UCSC Ensembl
Innerchr7:20316786..20320392hg19UCSC Ensembl
Innerchr7:20283311..20286917hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383607
hg193607
hg183607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5169480
SamplesNA18507
Known Genes
MethodSequencing
AnalysisCopy number variations are detected using the SOLiD Human CNV Tool. Regions with poor mappability are filtered out from consideration and a log ratio of coverage is used to determine areas of increased copy number. A Hidden Markov Model converts increased coverage into discrete copy number states.
PlatformNot specified
CommentsoriginalFile=Yoruban_cnv.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2519131
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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