A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969717



Internal ID18882789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151906928..151919028hg38UCSC Ensembl
OuterchrX:151075400..151087500hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812101
hg1912101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122270
Supporting Variants
SamplesKWS2
Known GenesMAGEA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969717
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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