A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002204



Internal ID19091421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119456171..119491214hg38UCSC Ensembl
Innerchr1:119998794..120033837hg19UCSC Ensembl
Innerchr1:119800317..119835360hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3835044
hg1935044
hg1835044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv299n100
Supporting Variantsnssv3484617
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)nsv1002204
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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