A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11335897



Internal ID3557537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7545919..7546560hg38UCSC Ensembl
Innerchr4:7545969..7546510hg38UCSC Ensembl
Outerchr4:7545866..7546613hg38UCSC Ensembl
chr4:7547646..7548287hg19UCSC Ensembl
Innerchr4:7547696..7548237hg19UCSC Ensembl
Outerchr4:7547593..7548340hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599529
Supporting Variants
SamplesHG03136
Known GenesSORCS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11335897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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