A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517572



Internal ID15444865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34973043..35012937hg38UCSC Ensembl
InnerchrX:34991160..35031054hg19UCSC Ensembl
InnerchrX:34901081..34940975hg18UCSC Ensembl
InnerchrX:34750817..34790711hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3839895
hg1939895
hg1839895
hg1739895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652413, nssv664226, nssv659649
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517572
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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