A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6231684



Internal ID9518448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174003125..174007127hg38UCSC Ensembl
chr1:173972263..173976265hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg384003
hg194003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662509
Supporting Variants
SamplesNA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6231684
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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