A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998796



Internal ID19158332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203961670..204000057hg38UCSC Ensembl
Innerchr1:203930798..203969185hg19UCSC Ensembl
Innerchr1:202197421..202235808hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3838388
hg1938388
hg1838388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705496
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)nsv998796
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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