A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670331



Internal ID9936436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15122744..15207038hg38UCSC Ensembl
Outerchr7:15122707..15207088hg38UCSC Ensembl
Innerchr7:15162369..15246663hg19UCSC Ensembl
Outerchr7:15162332..15246713hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3884382
hg1984382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6476953
SamplesHG00701
Known GenesAGMO
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670331
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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