A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966581



Internal ID19238778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:148547102..148547306hg38UCSC Ensembl
OuterchrX:147628623..147628827hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112491
Supporting Variants
SamplesKWS2
Known GenesAFF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966581
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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