A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658616



Internal ID15395268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76909582..76922212hg38UCSC Ensembl
InnerchrX:76130008..76142637hg19UCSC Ensembl
InnerchrX:76046402..76059032hg18UCSC Ensembl
InnerchrX:75912698..75925328hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3812631
hg1912630
hg1812631
hg1712631
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515864
Supporting Variants
Samples
Known GenesMIR384
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658616
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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