A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644225



Internal ID6684293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34998393..35001699hg38UCSC Ensembl
Innerchr19:34998457..35001635hg38UCSC Ensembl
Outerchr19:34998329..35001763hg38UCSC Ensembl
chr19:35489297..35492603hg19UCSC Ensembl
Innerchr19:35489361..35492539hg19UCSC Ensembl
Outerchr19:35489233..35492667hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16045265
SamplesHG03950
Known GenesGRAMD1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644225
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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