A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704256



Internal ID15440908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:50616088..50636075hg38UCSC Ensembl
InnerchrX:50359088..50379075hg19UCSC Ensembl
InnerchrX:50375828..50395815hg18UCSC Ensembl
InnerchrX:50192124..50212111hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3819988
hg1919988
hg1819988
hg1719988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527767
Supporting Variants
Samples
Known GenesSHROOM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704256
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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