A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959320



Internal ID18864871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:30868481..30868550hg38UCSC Ensembl
OuterchrX:30886598..30886667hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110077
Supporting Variants
SamplesKWS1
Known GenesTAB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959320
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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