A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6361158



Internal ID9338561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30439232..30445298hg38UCSC Ensembl
chr7:30478848..30484914hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg386067
hg196067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665927
Supporting Variants
SamplesNA19435
Known GenesNOD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6361158
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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