A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701711



Internal ID15438363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95357168..95720263hg38UCSC Ensembl
InnerchrX:94612167..94975262hg19UCSC Ensembl
InnerchrX:94498823..94861918hg18UCSC Ensembl
InnerchrX:94418312..94781407hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38363096
hg19363096
hg18363096
hg17363096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525572
Supporting Variants
Samples
Known GenesMIR548AE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701711
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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