A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585957



Internal ID6973476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47566970..47571878hg38UCSC Ensembl
Innerchr1:47566975..47571874hg38UCSC Ensembl
Outerchr1:47566966..47571883hg38UCSC Ensembl
chr1:48032642..48037550hg19UCSC Ensembl
Innerchr1:48032647..48037546hg19UCSC Ensembl
Outerchr1:48032638..48037555hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg384909
hg194909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9926607
SamplesHG00334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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