A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10915269



Internal ID5590180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7288443..7289264hg38UCSC Ensembl
Innerchr3:7288465..7289242hg38UCSC Ensembl
Outerchr3:7288421..7289286hg38UCSC Ensembl
chr3:7330130..7330951hg19UCSC Ensembl
Innerchr3:7330152..7330929hg19UCSC Ensembl
Outerchr3:7330108..7330973hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595185
Supporting Variants
SamplesNA19027
Known GenesGRM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10915269
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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