A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1821



Internal ID15541104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:7586724..7619068hg38UCSC Ensembl
OuterchrX:7504765..7537109hg19UCSC Ensembl
OuterchrX:7514765..7547109hg18UCSC Ensembl
OuterchrX:7364501..7396845hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg387678
hg197678
hg187678
hg177678
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6784
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)nssv1821
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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