A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004104



Internal ID19093321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:170593942..170642401hg38UCSC Ensembl
Innerchr1:170563083..170611542hg19UCSC Ensembl
Innerchr1:168829707..168878166hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3848460
hg1948460
hg1848460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484645, nssv3484157
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004104
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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