A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663820



Internal ID9929925
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 StatusM
Merged Variants
Supporting Variantsessv6492002, essv5660348, essv5985863
SamplesNA19920, NA19385, NA19257
Known GenesZC4H2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663820
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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