A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5985863



Internal ID9812284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64946397..64946750hg38UCSC Ensembl
chrX:64166277..64166630hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663820
Supporting Variants
SamplesNA19920
Known GenesZC4H2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5985863
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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