A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13013860



Internal ID3015676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152320471..152325394hg38UCSC Ensembl
Innerchr7:152320471..152325394hg38UCSC Ensembl
Outerchr7:152320140..152325685hg38UCSC Ensembl
chr7:152017556..152022479hg19UCSC Ensembl
Innerchr7:152017556..152022479hg19UCSC Ensembl
Outerchr7:152017225..152022770hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615502
Supporting Variants
SamplesNA20822
Known GenesKMT2C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13013860
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