A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997894



Internal ID19157430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:238329582..238451915hg38UCSC Ensembl
Innerchr1:238492882..238615215hg19UCSC Ensembl
Innerchr1:236559505..236681838hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38122334
hg19122334
hg18122334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3485677
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)nsv997894
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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