A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701611



Internal ID15438263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69003290..69051331hg38UCSC Ensembl
InnerchrX:68223133..68271174hg19UCSC Ensembl
InnerchrX:68139858..68187899hg18UCSC Ensembl
InnerchrX:68006154..68054195hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3848042
hg1948042
hg1848042
hg1748042
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519568
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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