A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6386761



Internal ID9628516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209904710..209912632hg38UCSC Ensembl
chr1:210078055..210085977hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg387923
hg197923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671575
Supporting Variants
SamplesNA19350
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6386761
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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