A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6541782



Internal ID9642138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24166203..24166827hg38UCSC Ensembl
OuterchrX:24166166..24166877hg38UCSC Ensembl
InnerchrX:24184320..24184944hg19UCSC Ensembl
OuterchrX:24184283..24184994hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674864
Supporting Variants
SamplesNA19375
Known GenesZFX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6541782
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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