A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595234



Internal ID6982552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9196941..9198779hg38UCSC Ensembl
Innerchr3:9196960..9198760hg38UCSC Ensembl
Outerchr3:9196922..9198798hg38UCSC Ensembl
chr3:9238625..9240463hg19UCSC Ensembl
Innerchr3:9238644..9240444hg19UCSC Ensembl
Outerchr3:9238606..9240482hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381839
hg191839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10917557
SamplesHG01694
Known GenesSRGAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595234
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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