A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011740



Internal ID19100958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92982922..93152812hg38UCSC Ensembl
Innerchr4:93904073..94073963hg19UCSC Ensembl
Innerchr4:94123096..94292986hg18UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38169891
hg19169891
hg18169891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742894
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)nsv1011740
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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