A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764844



Internal ID18961434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13881780..13883881hg38UCSC Ensembl
chrX:13899899..13902000hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075308
Supporting Variants
SamplesKWP1
Known GenesGPM6B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764844
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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