A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525288



Internal ID15452581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:36966468..36969871hg38UCSC Ensembl
Innerchr6:36934244..36937647hg19UCSC Ensembl
Innerchr6:37042222..37045625hg18UCSC Ensembl
Innerchr6:37042222..37045625hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg383404
hg193404
hg183404
hg173404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701393
Samples
Known GenesMTCH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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