A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6440402



Internal ID9170778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1607754..1613590hg38UCSC Ensembl
OuterchrX:1607717..1613640hg38UCSC Ensembl
InnerchrX:1726647..1732483hg19UCSC Ensembl
OuterchrX:1726610..1732533hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385924
hg195924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677663
Supporting Variants
SamplesHG01375
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6440402
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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