A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1822



Internal ID15541105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:7811986..7838943hg38UCSC Ensembl
OuterchrX:7780027..7806984hg19UCSC Ensembl
OuterchrX:7740027..7766984hg18UCSC Ensembl
OuterchrX:7589763..7616720hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg388977
hg198977
hg188977
hg178977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6785
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1822
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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