A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615601



Internal ID7002490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154299968..154351475hg38UCSC Ensembl
Innerchr7:154300468..154350975hg38UCSC Ensembl
Outerchr7:154298968..154352475hg38UCSC Ensembl
chr7:153997053..154048560hg19UCSC Ensembl
Innerchr7:153997553..154048060hg19UCSC Ensembl
Outerchr7:153996053..154049560hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3851508
hg1951508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1346e214
Supporting Variantsessv13027585
SamplesHG02953
Known GenesDPP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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