A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612570



Internal ID6999470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24261007..24274398hg38UCSC Ensembl
Innerchr7:24261007..24274398hg38UCSC Ensembl
Outerchr7:24260792..24274617hg38UCSC Ensembl
chr7:24300626..24314017hg19UCSC Ensembl
Innerchr7:24300626..24314017hg19UCSC Ensembl
Outerchr7:24300411..24314236hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3813392
hg1913392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12707051, essv12707053, essv12707054, essv12707042, essv12707044, essv12707045, essv12707055, essv12707049, essv12707050, essv12707043, essv12707052, essv12707048, essv12707047, essv12707046
SamplesHG01986, NA18502, NA19204, NA18877, HG03583, HG03547, HG02537, HG03391, HG03565, HG02971, HG02053, HG03351, HG01914, HG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612570
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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