A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072760



Internal ID18971897
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 StatusM
Merged Variants
Supporting Variantsnssv3762549
SamplesKWP1
Known GenesBAIAP2, BAIAP2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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