A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660663



Internal ID15397315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76909582..76923979hg38UCSC Ensembl
InnerchrX:76130008..76144404hg19UCSC Ensembl
InnerchrX:76046402..76060798hg18UCSC Ensembl
InnerchrX:75912698..75927094hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3814398
hg1914397
hg1814397
hg1714397
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)nssv660663
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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