A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6018895



Internal ID9532727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170702730..170704201hg38UCSC Ensembl
chr5:170129734..170131205hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659282
Supporting Variants
SamplesNA19063
Known GenesKCNIP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6018895
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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