A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv523n21



Internal ID20132244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113183439..114588429hg38UCSC Ensembl
chrX:112426666..113822902hg19UCSC Ensembl
chrX:112313322..113729158hg18UCSC Ensembl
chrX:112232811..113645882hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381404991
hg191396237
hg181415837
hg171413072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525517, nsv526494
Samples
Known GenesHTR2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv523n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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