A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033743



Internal ID19122964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3355602..3454490hg38UCSC Ensembl
Innerchr7:3395234..3494122hg19UCSC Ensembl
Innerchr7:3361760..3460648hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3898889
hg1998889
hg1898889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6222n100
Supporting Variantsnssv3654984
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)nsv1033743
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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