A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997718



Internal ID19157255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61190675..61237301hg38UCSC Ensembl
Innerchr3:61176349..61222975hg19UCSC Ensembl
Innerchr3:61151389..61198015hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3846627
hg1946627
hg1846627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593432
Samples
Known GenesFHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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