A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517690



Internal ID15444983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112441300..112477734hg38UCSC Ensembl
InnerchrX:111684528..111720962hg19UCSC Ensembl
InnerchrX:111571184..111607618hg18UCSC Ensembl
InnerchrX:111490673..111527107hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3836435
hg1936435
hg1836435
hg1736435
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655493, nssv684896, nssv657677, nssv652850, nssv675787, nssv653269
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517690
Frequency
Sample Size2026
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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