A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149690



Internal ID15534120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8106586..8147661hg38UCSC Ensembl
Innerchr17:8009904..8050979hg19UCSC Ensembl
Innerchr17:7950629..7991704hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3841076
hg1941076
hg1841076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574335
Supporting Variants
SamplesNINDS_3
Known GenesALOXE3, HES7, MIR6883, PER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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