A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601525



Internal ID6988562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97747145..97809414hg38UCSC Ensembl
Innerchr4:97747145..97809414hg38UCSC Ensembl
Outerchr4:97746645..97809914hg38UCSC Ensembl
chr4:98668296..98730565hg19UCSC Ensembl
Innerchr4:98668296..98730565hg19UCSC Ensembl
Outerchr4:98667796..98731065hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3862270
hg1962270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11541554
SamplesHG00436
Known GenesSTPG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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