A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9792



Internal ID15539850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:21024095..21085117hg38UCSC Ensembl
OuterchrY:23185981..23247003hg19UCSC Ensembl
OuterchrY:21595369..21656391hg18UCSC Ensembl
OuterchrY:21524106..21585128hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3861023
hg1961023
hg1861023
hg1761023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7474
Supporting Variants
SamplesNA18507
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)nssv9792
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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