A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5951281



Internal ID8928684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155804633..155983132hg38UCSC Ensembl
OuterchrX:155804476..155983285hg38UCSC Ensembl
InnerchrX:155034296..155212797hg19UCSC Ensembl
OuterchrX:155034139..155212950hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38178810
hg19178812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664638
Supporting Variants
SamplesNA18535
Known GenesVAMP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5951281
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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