A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656995



Internal ID9923100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12041937..12042201hg38UCSC Ensembl
Outerchr6:12041780..12042354hg38UCSC Ensembl
Innerchr6:12042170..12042434hg19UCSC Ensembl
Outerchr6:12042013..12042587hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6488854, essv6111407, essv6022562
SamplesNA19350, HG01073, NA19390
Known GenesHIVEP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656995
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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