A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603305



Internal ID6990337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177453541..177465545hg38UCSC Ensembl
Innerchr4:177454041..177465045hg38UCSC Ensembl
Outerchr4:177452541..177466545hg38UCSC Ensembl
chr4:178374695..178386699hg19UCSC Ensembl
Innerchr4:178375195..178386199hg19UCSC Ensembl
Outerchr4:178373695..178387699hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3812005
hg1912005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11718933, essv11718934, essv11718947, essv11718939, essv11718935, essv11718943, essv11718932, essv11718946, essv11718940, essv11718938, essv11718941, essv11718944, essv11718937, essv11718942, essv11718936, essv11718945, essv11718948
SamplesHG02433, NA18917, NA18519, NA20320, NA20340, NA19239, NA19921, HG02449, HG01879, HG03563, NA18853, HG02332, HG01896, NA19309, NA18501, HG02013, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603305
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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