A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419462



Internal ID15583246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128798965..128801635hg38UCSC Ensembl
Innerchr7:128439019..128441689hg19UCSC Ensembl
Innerchr7:128226255..128228925hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382671
hg192671
hg182671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819324
Supporting Variants
SamplesAK1
Known GenesCCDC136
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nssv1419462
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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