A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16366



Internal ID15488499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143836068..143837709hg38UCSC Ensembl
Outerchr7:143835953..143838674hg38UCSC Ensembl
Innerchr7:143533161..143534802hg19UCSC Ensembl
Outerchr7:143533046..143535767hg19UCSC Ensembl
Innerchr7:143164094..143165735hg18UCSC Ensembl
Outerchr7:143163979..143166700hg18UCSC Ensembl
Innerchr7:142970809..142972450hg17UCSC Ensembl
Outerchr7:142970694..142973415hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382722
hg192722
hg182722
hg172722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8227
Supporting Variants
SamplesNA18552
Known GenesLOC154761
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv16366
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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