A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010934



Internal ID19100151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:98663947..98711760hg38UCSC Ensembl
Innerchr1:99129503..99177316hg19UCSC Ensembl
Innerchr1:98902091..98949904hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3847814
hg1947814
hg1847814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3470933
Samples
Known GenesSNX7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010934
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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