A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6258485



Internal ID9235888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75942469..75942991hg38UCSC Ensembl
chr7:75571787..75572309hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38523
hg19523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674423
Supporting Variants
SamplesNA19469
Known GenesPOR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6258485
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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