A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6034517



Internal ID9011920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10420419..10435855hg38UCSC Ensembl
chr12:10573018..10588454hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3815437
hg1915437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658678
Supporting Variants
SamplesHG00565
Known GenesKLRC2, KLRC3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6034517
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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