A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6102024



Internal ID9001984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37073235..37077555hg38UCSC Ensembl
chr6:37041011..37045331hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384321
hg194321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658699
Supporting Variants
SamplesHG00608
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6102024
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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