A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9637047



Internal ID13604706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156737694..156737713hg38UCSC Ensembl
Innerchr7:156737690..156737717hg38UCSC Ensembl
Outerchr7:156737671..156737736hg38UCSC Ensembl
chr7:156530388..156530407hg19UCSC Ensembl
Innerchr7:156530384..156530411hg19UCSC Ensembl
Outerchr7:156530365..156530430hg19UCSC Ensembl
chr7:156223149..156223168hg18UCSC Ensembl
Innerchr7:156223172..156223145hg18UCSC Ensembl
Outerchr7:156223126..156223191hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3337565
Supporting Variants
SamplesNA12814
Known GenesLMBR1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9637047
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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