A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612672



Internal ID6652885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28431220..28436644hg38UCSC Ensembl
Innerchr7:28431220..28436644hg38UCSC Ensembl
Outerchr7:28431147..28436680hg38UCSC Ensembl
chr7:28470839..28476263hg19UCSC Ensembl
Innerchr7:28470839..28476263hg19UCSC Ensembl
Outerchr7:28470766..28476299hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg385425
hg195425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12714871
SamplesHG00737
Known GenesCREB5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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