A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13651997



Internal ID2703483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135523349..135533391hg38UCSC Ensembl
Innerchr9:135523384..135533356hg38UCSC Ensembl
Outerchr9:135523314..135533426hg38UCSC Ensembl
chr9:138415195..138425237hg19UCSC Ensembl
Innerchr9:138415230..138425202hg19UCSC Ensembl
Outerchr9:138415160..138425272hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3810043
hg1910043
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621994
Supporting Variants
SamplesHG02389
Known GenesLCN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13651997
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