A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9899592



Internal ID6524885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34883656..34884595hg38UCSC Ensembl
Innerchr1:34883657..34884595hg38UCSC Ensembl
Outerchr1:34883656..34884596hg38UCSC Ensembl
chr1:35349257..35350196hg19UCSC Ensembl
Innerchr1:35349258..35350196hg19UCSC Ensembl
Outerchr1:35349257..35350197hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585712
Supporting Variants
SamplesHG02973
Known GenesDLGAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9899592
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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