A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9935845



Internal ID1365094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55272690..55296711hg38UCSC Ensembl
Innerchr1:55272690..55296711hg38UCSC Ensembl
Outerchr1:55272190..55297211hg38UCSC Ensembl
chr1:55738363..55762384hg19UCSC Ensembl
Innerchr1:55738363..55762384hg19UCSC Ensembl
Outerchr1:55737863..55762884hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3824022
hg1924022
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3586110
Supporting Variants
SamplesHG01204
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9935845
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer