A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2752



Internal ID15195134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:5199747..5233952hg38UCSC Ensembl
Outerchr7:5239378..5273583hg19UCSC Ensembl
Outerchr7:5205904..5240109hg18UCSC Ensembl
Outerchr7:5012619..5046824hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg385819
hg195819
hg185819
hg175819
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627
Supporting Variants
SamplesNA18555
Known GenesWIPI2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2752
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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