A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697557



Internal ID18995838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93609987..93640465hg38UCSC Ensembl
Innerchr9:96372269..96402747hg19UCSC Ensembl
Innerchr9:95412090..95442568hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3830479
hg1930479
hg1830479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055035
Supporting Variants
Samples
Known GenesPHF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3697557
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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