A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762549



Internal ID18960298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81034599..81035700hg38UCSC Ensembl
chr17:79008399..79009500hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072760
Supporting Variants
SamplesKWP1
Known GenesBAIAP2, BAIAP2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762549
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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