A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6068638



Internal ID9630893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175153480..175153708hg38UCSC Ensembl
chr1:175122616..175122844hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676361
Supporting Variants
SamplesNA19355
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6068638
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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