A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984705



Internal ID19222618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:38705347..38705747hg38UCSC Ensembl
Outerchr17:36861600..36862000hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126456
Supporting Variants
SamplesKWS1
Known GenesMLLT6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984705
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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