A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061222



Internal ID18803753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15769620..16096464hg38UCSC Ensembl
Innerchr17:15672934..15999778hg19UCSC Ensembl
Innerchr17:15613659..15940503hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38326845
hg19326845
hg18326845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3107n100
Supporting Variantsnssv3719933
Samples
Known GenesADORA2B, MEIS3P1, NCOR1, TTC19, ZSWIM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061222
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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