A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614369



Internal ID6654575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103099307..103105188hg38UCSC Ensembl
Innerchr7:103099363..103105132hg38UCSC Ensembl
Outerchr7:103099251..103105244hg38UCSC Ensembl
chr7:102739754..102745635hg19UCSC Ensembl
Innerchr7:102739810..102745579hg19UCSC Ensembl
Outerchr7:102739698..102745691hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385882
hg195882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12912203
SamplesHG01883
Known GenesARMC10, NAPEPLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614369
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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