A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697571



Internal ID18649166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97695827..97836983hg38UCSC Ensembl
Innerchr9:100458109..100599265hg19UCSC Ensembl
Innerchr9:99497930..99639086hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38141157
hg19141157
hg18141157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043753
Supporting Variants
Samples
Known GenesXPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697571
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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