A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613295



Internal ID6653506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57174990..57198402hg38UCSC Ensembl
Innerchr7:57175490..57197902hg38UCSC Ensembl
Outerchr7:57173990..57199402hg38UCSC Ensembl
chr7:57242697..57266109hg19UCSC Ensembl
Innerchr7:57243197..57265609hg19UCSC Ensembl
Outerchr7:57241697..57267109hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3823413
hg1923413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12793689, essv12793690, essv12793688
SamplesNA20294, NA19835, HG03731
Known GenesGUSBP10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613295
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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