A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598396



Internal ID6985532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160962484..160968224hg38UCSC Ensembl
Innerchr3:160962484..160968224hg38UCSC Ensembl
Outerchr3:160962207..160968458hg38UCSC Ensembl
chr3:160680272..160686012hg19UCSC Ensembl
Innerchr3:160680272..160686012hg19UCSC Ensembl
Outerchr3:160679995..160686246hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385741
hg195741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199945, essv11199943, essv11199946, essv11199948, essv11199942, essv11199949, essv11199941, essv11199947, essv11199953, essv11199951, essv11199950, essv11199944, essv11199952
SamplesNA19664, HG00641, HG00637, NA12489, HG01095, HG01092, HG01921, NA19749, HG01395, HG00174, HG01111, NA07000, HG01516
Known GenesPPM1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598396
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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