A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677399



Internal ID9943504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30491562..30491852hg38UCSC Ensembl
Outerchr10:30491525..30491902hg38UCSC Ensembl
Innerchr10:30780491..30780781hg19UCSC Ensembl
Outerchr10:30780454..30780831hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6325701
SamplesNA12751
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677399
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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