A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037172



Internal ID19126391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135996295..136047043hg38UCSC Ensembl
Innerchr9:138888141..138938889hg19UCSC Ensembl
Innerchr9:138027962..138078710hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3850749
hg1950749
hg1850749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696508
Samples
Known GenesNACC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037172
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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