A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7484



Internal ID15552498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:88797991..88839915hg38UCSC Ensembl
Outerchr10:90557748..90599672hg19UCSC Ensembl
Outerchr10:90547728..90589652hg18UCSC Ensembl
Outerchr10:90547728..90589652hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388150
hg198150
hg188150
hg178150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6406, nssv10772
SamplesNA12156, NA18956
Known GenesANKRD22, LIPM
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)nsv7484
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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