A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976981



Internal ID19244636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:21953902..21953963hg38UCSC Ensembl
OuterchrX:21972020..21972081hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139393
Supporting Variants
SamplesKWS2
Known GenesSMS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976981
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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