A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5931739



Internal ID9362380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62516798..62695300hg38UCSC Ensembl
OuterchrX:62516764..62695335hg38UCSC Ensembl
InnerchrX:61736268..61914770hg19UCSC Ensembl
OuterchrX:61736234..61914805hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38178572
hg19178572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664307
Supporting Variants
SamplesNA18557
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5931739
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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