A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567885



Internal ID18519480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81416389..81473664hg38UCSC Ensembl
Innerchr17:79390189..79440690hg19UCSC Ensembl
Innerchr17:77004784..77055285hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3857276
hg1950502
hg1850502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058786
Supporting Variants
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567885
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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