A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567752



Internal ID18866033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68082268..68183009hg38UCSC Ensembl
Innerchr17:66078392..66179150hg19UCSC Ensembl
Innerchr17:63590029..63690745hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38100742
hg19100759
hg18100717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056977
Supporting Variants
Samples
Known GenesLINC00674
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567752
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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