A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126951



Internal ID18908910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:150983327..150984927hg38UCSC Ensembl
OuterchrX:150151800..150153400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4318n106
Supporting Variantsnssv3985234
SamplesKWS1
Known GenesHMGB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126951
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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