A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3433151



Internal ID15280107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87351504..87351523hg38UCSC Ensembl
Innerchr7:87351500..87351527hg38UCSC Ensembl
Outerchr7:87351481..87351546hg38UCSC Ensembl
chr7:86980820..86980839hg19UCSC Ensembl
Innerchr7:86980816..86980843hg19UCSC Ensembl
Outerchr7:86980797..86980862hg19UCSC Ensembl
chr7:86818756..86818775hg18UCSC Ensembl
Innerchr7:86818779..86818752hg18UCSC Ensembl
Outerchr7:86818733..86818798hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9634925
SamplesNA19141
Known GenesCROT
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3433151
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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