A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12559788



Internal ID4053835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135518556..135550084hg38UCSC Ensembl
chr6:135839694..135871222hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3831529
hg1931529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610897
Supporting Variants
SamplesHG03694
Known GenesLINC00271
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12559788
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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