A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749030



Internal ID18700625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10516796..10567176hg38UCSC Ensembl
Innerchr6:10517029..10567409hg19UCSC Ensembl
Innerchr6:10625015..10675395hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3850381
hg1950381
hg1850381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030024
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749030
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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