A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013199



Internal ID19102417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92474358..92589901hg38UCSC Ensembl
Innerchr4:93395509..93511052hg19UCSC Ensembl
Innerchr4:93614532..93730075hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38115544
hg19115544
hg18115544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5338n100
Supporting Variantsnssv3742891
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013199
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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