A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12922840



Internal ID5951234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109522440..109524038hg38UCSC Ensembl
Innerchr7:109522440..109524038hg38UCSC Ensembl
Outerchr7:109522379..109524088hg38UCSC Ensembl
chr7:109162497..109164095hg19UCSC Ensembl
Innerchr7:109162497..109164095hg19UCSC Ensembl
Outerchr7:109162436..109164145hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381599
hg191599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614501
Supporting Variants
SamplesNA19372
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12922840
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