A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984346



Internal ID19214319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44531292..44531399hg38UCSC Ensembl
OuterchrX:44390538..44390645hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126138
Supporting Variants
SamplesKWS1
Known GenesFUNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984346
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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