A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6825



Internal ID15205087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:19549435..19583087hg38UCSC Ensembl
OuterchrX:19567553..19601205hg19UCSC Ensembl
OuterchrX:19477474..19511126hg18UCSC Ensembl
OuterchrX:19327210..19360862hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg385786
hg195786
hg185786
hg175786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8696
SamplesNA12156
Known GenesSH3KBP1
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)nsv6825
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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