A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567700



Internal ID18865981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57210510..57226803hg38UCSC Ensembl
Innerchr17:55287871..55304164hg19UCSC Ensembl
Innerchr17:52642870..52659163hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3816294
hg1916294
hg1816294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055884
Supporting Variants
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)nssv3567700
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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