A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960433



Internal ID18873561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44531247..44531335hg38UCSC Ensembl
OuterchrX:44390493..44390581hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128534
Supporting Variants
SamplesKWS1
Known GenesFUNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960433
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer