A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976336



Internal ID18890816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120374770..120374822hg38UCSC Ensembl
OuterchrX:119508625..119508677hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115287
Supporting Variants
SamplesKWS2
Known GenesATP1B4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976336
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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