A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986799



Internal ID19219661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:25929837..25930163hg38UCSC Ensembl
OuterchrX:25947954..25948280hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132119
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986799
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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