A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649852



Internal ID18601447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99839200..100082800hg38UCSC Ensembl
Innerchr6:100287076..100530676hg19UCSC Ensembl
Innerchr6:100393797..100637397hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38243601
hg19243601
hg18243601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024904
Supporting Variants
Samples
Known GenesMCHR2, MCHR2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649852
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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