A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10152544



Internal ID3786024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155689908..155694673hg38UCSC Ensembl
Innerchr1:155689908..155694673hg38UCSC Ensembl
Outerchr1:155689498..155695048hg38UCSC Ensembl
chr1:155659699..155664464hg19UCSC Ensembl
Innerchr1:155659699..155664464hg19UCSC Ensembl
Outerchr1:155659289..155664839hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg384766
hg194766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587631
Supporting Variants
SamplesHG03436
Known GenesDAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10152544
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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