A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13038273



Internal ID2297438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156018036..156030460hg38UCSC Ensembl
Innerchr7:156018086..156030410hg38UCSC Ensembl
Outerchr7:156017986..156030510hg38UCSC Ensembl
chr7:155810730..155823154hg19UCSC Ensembl
Innerchr7:155810780..155823104hg19UCSC Ensembl
Outerchr7:155810680..155823204hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3812425
hg1912425
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615646
Supporting Variants
SamplesHG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13038273
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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