A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110084



Internal ID19250013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:54547180..54547244hg38UCSC Ensembl
OuterchrX:54573613..54573677hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959329
SamplesKWS1
Known GenesGNL3L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110084
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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