A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv464188



Internal ID15524253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167935400..168198653hg38UCSC Ensembl
Innerchr6:168336080..168599333hg19UCSC Ensembl
Innerchr6:168078929..168342182hg18UCSC Ensembl
Innerchr6:168154636..168417889hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38263254
hg19263254
hg18263254
hg17263254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv791n27
Supporting Variantsnssv540141
Samples1780854556_A
Known GenesFRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv464188
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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