A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612880



Internal ID6999779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38359349..38362052hg38UCSC Ensembl
Innerchr7:38359384..38362017hg38UCSC Ensembl
Outerchr7:38359314..38362087hg38UCSC Ensembl
chr7:38398950..38401653hg19UCSC Ensembl
Innerchr7:38398985..38401618hg19UCSC Ensembl
Outerchr7:38398915..38401688hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12742816, essv12742809, essv12742810, essv12742812, essv12742813, essv12742814, essv12742811, essv12742815, essv12742807, essv12742808
SamplesNA19332, NA20274, NA18486, HG02620, HG02642, NA19921, NA19982, NA19625, HG03072, HG01516
Known GenesTRG-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612880
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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