A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995044



Internal ID19210039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137590148..137590648hg38UCSC Ensembl
Outerchr9:140484600..140485100hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144306
Supporting Variants
SamplesKWS1
Known GenesZMYND19
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995044
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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