A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6521685



Internal ID8891700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62769099..62780614hg38UCSC Ensembl
OuterchrX:62769062..62780664hg38UCSC Ensembl
InnerchrX:61988569..62000084hg19UCSC Ensembl
OuterchrX:61988532..62000134hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3811603
hg1911603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667243
Supporting Variants
SamplesHG00339
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6521685
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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