A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13037756



Internal ID3082970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155943583..155946042hg38UCSC Ensembl
Innerchr7:155943614..155946011hg38UCSC Ensembl
Outerchr7:155943552..155946073hg38UCSC Ensembl
chr7:155736277..155738736hg19UCSC Ensembl
Innerchr7:155736308..155738705hg19UCSC Ensembl
Outerchr7:155736246..155738767hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382460
hg192460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615641
Supporting Variants
SamplesHG02702
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13037756
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