A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5936295



Internal ID9909534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35682072..35685358hg38UCSC Ensembl
chr7:35721682..35724968hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg383287
hg193287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659669
Supporting Variants
SamplesNA20805
Known GenesHERPUD2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5936295
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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