A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067328



Internal ID18809859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78595683..78658916hg38UCSC Ensembl
Innerchr17:76591765..76654998hg19UCSC Ensembl
Innerchr17:74103360..74166593hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3863234
hg1963234
hg1863234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3285n100
Supporting Variantsnssv3567821, nssv3567822
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067328
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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