A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615344



Internal ID7002233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145479205..145529481hg38UCSC Ensembl
Innerchr7:145479235..145529451hg38UCSC Ensembl
Outerchr7:145479175..145529511hg38UCSC Ensembl
chr7:145176298..145226574hg19UCSC Ensembl
Innerchr7:145176328..145226544hg19UCSC Ensembl
Outerchr7:145176268..145226604hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3850277
hg1950277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12995957
SamplesHG02420
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615344
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer