A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6571007



Internal ID9570550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123181755..123182293hg38UCSC Ensembl
OuterchrX:123181598..123182446hg38UCSC Ensembl
InnerchrX:122315608..122316146hg19UCSC Ensembl
OuterchrX:122315451..122316299hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675277
Supporting Variants
SamplesNA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6571007
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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