A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696361



Internal ID18994642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74218561..74286052hg38UCSC Ensembl
Innerchr9:76833477..76900968hg19UCSC Ensembl
Innerchr9:76023297..76090788hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3867492
hg1967492
hg1867492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043800
Supporting Variants
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696361
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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