A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7528



Internal ID15536336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:99965154..99998777hg38UCSC Ensembl
Outerchr2:100581616..100615239hg19UCSC Ensembl
Outerchr2:99948048..99981671hg18UCSC Ensembl
Outerchr2:100040134..100073757hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg385809
hg195809
hg185809
hg175809
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2846
Supporting Variants
SamplesNA12156
Known GenesAFF3
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)nssv7528
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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