A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600485



Internal ID6987528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51951703..51971534hg38UCSC Ensembl
Innerchr4:51951703..51971534hg38UCSC Ensembl
Outerchr4:51951203..51972034hg38UCSC Ensembl
chr4:52817869..52837700hg19UCSC Ensembl
Innerchr4:52817869..52837700hg19UCSC Ensembl
Outerchr4:52817369..52838200hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3819832
hg1919832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11430699
SamplesHG02019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600485
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