A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119645



Internal ID19278547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:149938682..149939682hg38UCSC Ensembl
OuterchrX:149106900..149107900hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4316n106
Supporting Variantsnssv3982088
SamplesKWS1
Known GenesLINC00894
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119645
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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