A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057945



Internal ID19147164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10525748..10570464hg38UCSC Ensembl
Innerchr17:10429065..10473781hg19UCSC Ensembl
Innerchr17:10369790..10414506hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3844717
hg1944717
hg1844717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560348
Samples
Known GenesMYH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057945
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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