A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10704



Internal ID15195408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49162987..49195244hg38UCSC Ensembl
OuterchrX:49017812..49051703hg19UCSC Ensembl
OuterchrX:48904756..48938647hg18UCSC Ensembl
OuterchrX:48774183..48808074hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3832258
hg1933892
hg1833892
hg1733892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7442
Supporting Variants
SamplesNA18956
Known GenesMAGIX, PLP2, PRICKLE3, SYP
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)nssv10704
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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