A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695666



Internal ID15054397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156237297..156238195hg38UCSC Ensembl
Innerchr7:156237296..156238196hg38UCSC Ensembl
Outerchr7:156236297..156239195hg38UCSC Ensembl
chr7:156029991..156030889hg19UCSC Ensembl
Innerchr7:156029990..156030890hg19UCSC Ensembl
Outerchr7:156028991..156031889hg19UCSC Ensembl
chr7:155722752..155723650hg18UCSC Ensembl
Innerchr7:155723651..155722751hg18UCSC Ensembl
Outerchr7:155721752..155724650hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3346379
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695666
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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