A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615117



Internal ID7002006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135306995..135308640hg38UCSC Ensembl
Innerchr7:135307009..135308627hg38UCSC Ensembl
Outerchr7:135306982..135308654hg38UCSC Ensembl
chr7:134991747..134993392hg19UCSC Ensembl
Innerchr7:134991761..134993379hg19UCSC Ensembl
Outerchr7:134991734..134993406hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381646
hg191646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12975956
SamplesHG01842
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615117
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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