A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019190



Internal ID19108408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3857002..3903934hg38UCSC Ensembl
Innerchr7:3896634..3943566hg19UCSC Ensembl
Innerchr7:3863160..3910092hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3846933
hg1946933
hg1846933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752794
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019190
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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