A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004836



Internal ID19094053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104561736..104630473hg38UCSC Ensembl
Innerchr1:105104358..105173095hg19UCSC Ensembl
Innerchr1:104905881..104974618hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3868738
hg1968738
hg1868738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv232n100
Supporting Variantsnssv3486273, nssv3701134
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)nsv1004836
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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