A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996210



Internal ID15581711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24254197..24446339hg38UCSC Ensembl
InnerchrX:24272314..24464456hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38192143
hg19192143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483074
Supporting Variants
Samples
Known GenesSUPT20HL1, SUPT20HL2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996210
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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