A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697541



Internal ID18995822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88852009..88938454hg38UCSC Ensembl
Innerchr9:91466924..91553369hg19UCSC Ensembl
Innerchr9:90656744..90743189hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3886446
hg1986446
hg1886446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054832
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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