A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526494



Internal ID15107101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113183439..114588429hg38UCSC Ensembl
InnerchrX:112426666..113822902hg19UCSC Ensembl
InnerchrX:112313322..113729158hg18UCSC Ensembl
InnerchrX: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 Variantsdgv523n21
Supporting Variantsnssv702803
Samples
Known GenesHTR2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526494
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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