A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877106



Internal ID16171062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81030816..81043967hg38UCSC Ensembl
Innerchr17:79004616..79017767hg19UCSC Ensembl
Innerchr17:76619211..76632362hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3813152
hg1913152
hg1813152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576169
Supporting Variants
Samples
Known GenesBAIAP2, BAIAP2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877106
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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