A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9636781



Internal ID13164678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149408535..149408554hg38UCSC Ensembl
Innerchr7:149408531..149408558hg38UCSC Ensembl
Outerchr7:149408512..149408577hg38UCSC Ensembl
chr7:149105626..149105645hg19UCSC Ensembl
Innerchr7:149105622..149105649hg19UCSC Ensembl
Outerchr7:149105603..149105668hg19UCSC Ensembl
chr7:148736559..148736578hg18UCSC Ensembl
Innerchr7:148736582..148736555hg18UCSC Ensembl
Outerchr7:148736536..148736601hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3380881
Supporting Variants
SamplesNA11840
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9636781
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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