A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3431145



Internal ID15278101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156237197..156238295hg38UCSC Ensembl
Innerchr7:156237295..156238197hg38UCSC Ensembl
Outerchr7:156236197..156239295hg38UCSC Ensembl
chr7:156029891..156030989hg19UCSC Ensembl
Innerchr7:156029989..156030891hg19UCSC Ensembl
Outerchr7:156028891..156031989hg19UCSC Ensembl
chr7:155722652..155723750hg18UCSC Ensembl
Innerchr7:155723652..155722750hg18UCSC Ensembl
Outerchr7:155721652..155724750hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4008e59
Supporting Variantsessv8695665
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3431145
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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